IL29495A - Catechol half esters of beta-haloethylphosphonic acid - Google Patents

Catechol half esters of beta-haloethylphosphonic acid

Info

Publication number: IL29495A
Authority: IL; Israel
Prior art keywords: catechol; beta; groups; half esters; compound
Prior art date: 1967-02-23

Application number

IL29495A

Other languages

English (en)

Original Assignee

Gen Aniline & Film Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1967-02-23

Filing date

1968-02-19

Publication date

1972-08-30

1968-02-19 Application filed by Gen Aniline & Film Corp filed Critical Gen Aniline & Film Corp

1972-08-30 Publication of IL29495A publication Critical patent/IL29495A/en

Links

YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 title description 25
150000002148 esters Chemical class 0.000 title description 21
239000002253 acid Substances 0.000 title description 5
150000001875 compounds Chemical class 0.000 claims description 18
125000005843 halogen group Chemical group 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 4
150000002790 naphthalenes Chemical class 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
125000001246 bromo group Chemical group Br* 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
150000002431 hydrogen Chemical class 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 12
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 7
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
244000046052 Phaseolus vulgaris Species 0.000 description 5
-1 cyclic ester Chemical class 0.000 description 5
235000010627 Phaseolus vulgaris Nutrition 0.000 description 4
238000000034 method Methods 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
244000075850 Avena orientalis Species 0.000 description 2
235000007319 Avena orientalis Nutrition 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
244000299507 Gossypium hirsutum Species 0.000 description 2
244000013123 dwarf bean Species 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000203 mixture Substances 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
239000000243 solution Substances 0.000 description 2
GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 1
150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
BFKXVERGWXHHIH-UHFFFAOYSA-N 2-bromoethylphosphonic acid Chemical compound OP(O)(=O)CCBr BFKXVERGWXHHIH-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
235000009432 Gossypium hirsutum Nutrition 0.000 description 1
241000209219 Hordeum Species 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
241000735234 Ligustrum Species 0.000 description 1
241000576411 Ligustrum ovalifolium Species 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
239000007866 anti-wear additive Substances 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
229940125758 compound 15 Drugs 0.000 description 1
235000005489 dwarf bean Nutrition 0.000 description 1
239000000975 dye Substances 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
GATNOFPXSDHULC-UHFFFAOYSA-N ethylphosphonic acid Chemical compound CCP(O)(O)=O GATNOFPXSDHULC-UHFFFAOYSA-N 0.000 description 1
229960004887 ferric hydroxide Drugs 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
230000012010 growth Effects 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
238000007689 inspection Methods 0.000 description 1
IEECXTSVVFWGSE-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Fe+3] IEECXTSVVFWGSE-UHFFFAOYSA-M 0.000 description 1
235000021332 kidney beans Nutrition 0.000 description 1
239000003921 oil Substances 0.000 description 1
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
238000000954 titration curve Methods 0.000 description 1
230000000007 visual effect Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4084—Esters with hydroxyaryl compounds
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Biochemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Life Sciences & Earth Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Cultivation Of Plants (AREA)

IL29495A 1967-02-23 1968-02-19 Catechol half esters of beta-haloethylphosphonic acid IL29495A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US61782067A	1967-02-23	1967-02-23

Publications (1)

Publication Number	Publication Date
IL29495A true IL29495A (en)	1972-08-30

Family

ID=24475196

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL29495A IL29495A (en)	1967-02-23	1968-02-19	Catechol half esters of beta-haloethylphosphonic acid

Country Status (6)

Country	Link
US (1)	US3531549A (de)
CH (1)	CH500231A (de)
DE (1)	DE1668181B2 (de)
FR (1)	FR1556007A (de)
GB (1)	GB1219801A (de)
IL (1)	IL29495A (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1950100B2 (de) *	1969-10-04	1976-12-02	Bayer Ag, 5090 Leverkusen	Verwendung von 2-chloraethan-(thiono)- phosphonsaeureamido-verbindungen zur beeinflussung des pflanzenwachstums
US3907540A (en) *	1969-10-04	1975-09-23	Bayer Ag	Herbicidal composition and method comploying 2-chloroethane-(thiono)phosphonic acid derivatives
US4401454A (en) *	1969-10-24	1983-08-30	Union Carbide Corporation	Growth regulation methods
US3879188A (en) *	1969-10-24	1975-04-22	Amchem Prod	Growth regulation process
US4240819A (en) *	1972-01-28	1980-12-23	Union Carbide Agricultural Products, Inc.	Method for the inhibition of plant growth
US4271072A (en) *	1977-12-20	1981-06-02	American Hoechst Corporation	Azo dyestuffs containing -SO2 CH2 CH2 OSO3 H and -N(CH2 CH2 OSO3 H)2 groups
HU190580B (en) *	1984-07-18	1986-09-29	Nitrokemia Ipartelepek,Hu	Plant growth regulating compositions comprising phosphonic acid-esters as active substance
US5994272A (en) *	1998-04-14	1999-11-30	Fresh Express Incorporated	Method for inhibition of head formation in lettuce

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3118876A (en) *	1958-07-26	1964-01-21	Takeda Pharmaceutical	Process for preparing glycoside phosphates

1967
- 1967-02-23 US US617820A patent/US3531549A/en not_active Expired - Lifetime
1968
- 1968-02-16 DE DE1668181A patent/DE1668181B2/de not_active Ceased
- 1968-02-19 CH CH234768A patent/CH500231A/de not_active IP Right Cessation
- 1968-02-19 IL IL29495A patent/IL29495A/en unknown
- 1968-02-22 GB GB8757/68A patent/GB1219801A/en not_active Expired
- 1968-02-23 FR FR1556007D patent/FR1556007A/fr not_active Expired

Also Published As

Publication number	Publication date
CH500231A (de)	1970-12-15
FR1556007A (de)	1969-01-31
US3531549A (en)	1970-09-29
GB1219801A (en)	1971-01-20
DE1668181A1 (de)	1971-08-05
DE1668181B2 (de)	1975-12-11

Publication	Publication Date	Title
EP0262209B1 (de)	1992-08-05	Synergetische pflanzenwuchsregulatorzusammensetzung
US4270948A (en)	1981-06-02	Herbicidal compound, herbicidal composition containing the same, and method of use thereof
JP2693774B2 (ja)	1997-12-24	マロン酸誘導体化合物の植物の成長を抑制するための使用
EP0109314A1 (de)	1984-05-23	Aluminium N-Phosphonomethylglyzin und seine Verwendung als Herbizid
IE51852B1 (en)	1987-04-15	Trialkylsulfonium and trialkylsulfoxonium salts of n-phosphonomethylglycine,production thereof,their use as plant growth regulators and herbicides and compositions containing them
IL47972A (en)	1977-12-30	N-phosphonomethylglycines and herbicidal compositions containing them
US4384880A (en)	1983-05-24	Trialkylsulfonium salts of N-phosphonomethyl-glycine and their use as plant growth regulators and herbicides
US4525202A (en)	1985-06-25	Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants
US3531549A (en)	1970-09-29	Catechol half esters of beta-haloethylphosphonic acid
US3551528A (en)	1970-12-29	Phosphonic acid esters and the methol for their preparation
US3223514A (en)	1965-12-14	Process for the control of plant growth
US4415503A (en)	1983-11-15	Method for preparation of N-phosphonomethylglycine
US4018854A (en)	1977-04-19	Carboxyphosphonates
EP0105262A1 (de)	1984-04-18	Tetrasubstituiertes ammoniumsalz aus n-phosphonomethylglycin und dessen verwendung als herbizide und pflanzenwachstumsregler
US3562363A (en)	1971-02-09	O-catechol o-hydrocarbyl-vinyl phosphonates and process for making same
GB631549A (en)	1949-11-04	Improvements in or relating to the manufacture of compounds containing phosphorus having insecticidal properties
US4191552A (en)	1980-03-04	Amine salts of substituted N-phosphonomethylureas and their use as plant growth regulators
US4376644A (en)	1983-03-15	Tri-mixed alkylsulfonium salts of N-phosphonomethylglycine and their use as plant growth regulators and herbicides
CA1131654A (en)	1982-09-14	Ester derivatives of n-trifluoroacetyl-n- phosphonomethylglycine and the herbicidal use thereof
US3388150A (en)	1968-06-11	Fluoroketone hemiketal esters
CA1122995A (en)	1982-05-04	Amide and hydrazide derivatives of n-trifluoroacetyl-n-phosphonomethylglycine
CA1134383A (en)	1982-10-26	Derivatives of n-trifluoroacetyl-n- phosphonomethylglycine dichloride
US3432495A (en)	1969-03-11	Aryl hydroxyalkyl arsinic acids and salts thereof
EP0068732B1 (de)	1985-08-28	Herbizid wirkende Monoester und Diester von N-alkyl substituierten Amino-Methyl Phosphonsäuren und Verfahren zu ihrer Herstellung
US4328027A (en)	1982-05-04	Di-triethylamine salt of N,N'-bis-carboethoxymethyl-N,N'-bis-phosphonomethylurea and its use as a plant growth regulator