GB785332A - Improvements in or relating to defoliants - Google Patents
Improvements in or relating to defoliantsInfo
- Publication number
- GB785332A GB785332A GB14578/55A GB1457855A GB785332A GB 785332 A GB785332 A GB 785332A GB 14578/55 A GB14578/55 A GB 14578/55A GB 1457855 A GB1457855 A GB 1457855A GB 785332 A GB785332 A GB 785332A
- Authority
- GB
- United Kingdom
- Prior art keywords
- butynediol
- butyne
- substituted
- hydroxy
- organic
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000002837 defoliant Substances 0.000 title 1
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 abstract 7
- 150000001875 compounds Chemical class 0.000 abstract 5
- -1 hydroxy, carboxy Chemical group 0.000 abstract 5
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 4
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- DLDJFQGPPSQZKI-UHFFFAOYSA-N but-2-yne-1,4-diol Chemical compound OCC#CCO DLDJFQGPPSQZKI-UHFFFAOYSA-N 0.000 abstract 3
- 125000000962 organic group Chemical group 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract 2
- 125000002723 alicyclic group Chemical group 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 150000001340 alkali metals Chemical class 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 230000003750 conditioning effect Effects 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 230000035613 defoliation Effects 0.000 abstract 2
- 150000002009 diols Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- KDOWHHULNTXTNS-UHFFFAOYSA-N hex-3-yne-2,5-diol Chemical compound CC(O)C#CC(C)O KDOWHHULNTXTNS-UHFFFAOYSA-N 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 150000002500 ions Chemical class 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- YXUIOVCVYTULFD-UHFFFAOYSA-N 1,4-diethoxyoct-2-yne Chemical compound CCCCC(OCC)C#CCOCC YXUIOVCVYTULFD-UHFFFAOYSA-N 0.000 abstract 1
- QTMJOSQOBGNKJU-UHFFFAOYSA-N 1,4-dimethoxybut-1-yne Chemical compound COCCC#COC QTMJOSQOBGNKJU-UHFFFAOYSA-N 0.000 abstract 1
- FEPWAORBSFQYME-UHFFFAOYSA-N 1-(4-methylphenyl)but-2-yne-1,4-diol Chemical compound CC1=CC=C(C(O)C#CCO)C=C1 FEPWAORBSFQYME-UHFFFAOYSA-N 0.000 abstract 1
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 abstract 1
- LJTTZAWYVIIPGH-UHFFFAOYSA-N 1-hexoxynon-1-yn-4-ol Chemical compound C(CCCCC)OC#CCC(CCCCC)O LJTTZAWYVIIPGH-UHFFFAOYSA-N 0.000 abstract 1
- NBHKOXMOIRGJAI-UHFFFAOYSA-N 1-phenylbut-2-yne-1,4-diol Chemical compound OCC#CC(O)C1=CC=CC=C1 NBHKOXMOIRGJAI-UHFFFAOYSA-N 0.000 abstract 1
- DCCCOSYHWHASIE-UHFFFAOYSA-N 1-phenylpent-2-yne-1,4-diol Chemical compound CC(O)C#CC(O)C1=CC=CC=C1 DCCCOSYHWHASIE-UHFFFAOYSA-N 0.000 abstract 1
- FHOQZOTZSZDBES-UHFFFAOYSA-N 2,7-dimethyloct-4-yne-3,6-diol Chemical compound CC(C)C(O)C#CC(O)C(C)C FHOQZOTZSZDBES-UHFFFAOYSA-N 0.000 abstract 1
- YPNPDIYVYYKUNS-UHFFFAOYSA-N 3-pentylbut-1-yne-1,4-diol Chemical compound C(CCCC)C(C#CO)CO YPNPDIYVYYKUNS-UHFFFAOYSA-N 0.000 abstract 1
- UGKOHLOLYBTFFD-UHFFFAOYSA-N 4-butoxybut-3-yn-1-ol Chemical compound C(CCC)OC#CCCO UGKOHLOLYBTFFD-UHFFFAOYSA-N 0.000 abstract 1
- MJJOLNIDJAYXPZ-UHFFFAOYSA-N 4-methoxybut-3-yn-1-ol Chemical compound COC#CCCO MJJOLNIDJAYXPZ-UHFFFAOYSA-N 0.000 abstract 1
- XZYBRZJIWHYCMQ-UHFFFAOYSA-N 5-methoxy-2-methyl-5-phenyldec-3-yn-2-ol Chemical compound COC(C#CC(O)(C)C)(C1=CC=CC=C1)CCCCC XZYBRZJIWHYCMQ-UHFFFAOYSA-N 0.000 abstract 1
- XOLACQIZUOBSBS-UHFFFAOYSA-N C(#CCCO)O.[Ca] Chemical compound C(#CCCO)O.[Ca] XOLACQIZUOBSBS-UHFFFAOYSA-N 0.000 abstract 1
- UWTXLRIDKUNASY-UHFFFAOYSA-N C(#CCCO)O.[K] Chemical compound C(#CCCO)O.[K] UWTXLRIDKUNASY-UHFFFAOYSA-N 0.000 abstract 1
- BCTGUQDUPJGZKG-UHFFFAOYSA-N C(#CCCO)O.[Na].[Na] Chemical compound C(#CCCO)O.[Na].[Na] BCTGUQDUPJGZKG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- FYPCWDDCCZBFMW-UHFFFAOYSA-N OCCC#CO.C1=CC=NC=C1 Chemical compound OCCC#CO.C1=CC=NC=C1 FYPCWDDCCZBFMW-UHFFFAOYSA-N 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 abstract 1
- XRCDXEHFFGTDAH-UHFFFAOYSA-N dec-2-yne-1,4-diol Chemical compound CCCCCCC(O)C#CCO XRCDXEHFFGTDAH-UHFFFAOYSA-N 0.000 abstract 1
- GQYLRBVRXXXXJR-UHFFFAOYSA-N dec-3-yne-2,5-diol Chemical compound CC(C#CC(O)CCCCC)O GQYLRBVRXXXXJR-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- DTVARWVRNUFXLQ-UHFFFAOYSA-N hept-3-yne-2,5-diol Chemical compound CCC(O)C#CC(C)O DTVARWVRNUFXLQ-UHFFFAOYSA-N 0.000 abstract 1
- PUAQPJSBIUZGNW-UHFFFAOYSA-N heptadec-3-yne-2,5-diol Chemical compound CC(C#CC(O)CCCCCCCCCCCC)O PUAQPJSBIUZGNW-UHFFFAOYSA-N 0.000 abstract 1
- SBFXIKAUMNVVCT-UHFFFAOYSA-N hex-2-yne-1,4-diol Chemical compound CCC(O)C#CCO SBFXIKAUMNVVCT-UHFFFAOYSA-N 0.000 abstract 1
- UBQGZSMUMHBGEH-UHFFFAOYSA-N hexadec-2-yne-1,4-diol Chemical compound C(CCCCCCCCCCC)C(C#CCO)O UBQGZSMUMHBGEH-UHFFFAOYSA-N 0.000 abstract 1
- DKKNCFNFVQVBJS-UHFFFAOYSA-N hexadec-6-yne-5,8-diol Chemical compound C(CCC)C(C#CC(O)CCCCCCCC)O DKKNCFNFVQVBJS-UHFFFAOYSA-N 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- WJWFPMLIEMSHQC-UHFFFAOYSA-N oct-2-yne-1,4-diol Chemical compound CCCCC(O)C#CCO WJWFPMLIEMSHQC-UHFFFAOYSA-N 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
- C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
- C07C29/42—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones with compounds containing triple carbon-to-carbon bonds, e.g. with metal-alkynes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Detergent Compositions (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US344592XA | 1954-05-20 | 1954-05-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB785332A true GB785332A (en) | 1957-10-23 |
Family
ID=21876559
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB14578/55A Expired GB785332A (en) | 1954-05-20 | 1955-05-20 | Improvements in or relating to defoliants |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE538246A (th) |
| CH (1) | CH344592A (th) |
| FR (1) | FR1131562A (th) |
| GB (1) | GB785332A (th) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20170077508A (ko) * | 2015-12-28 | 2017-07-06 | 주식회사 대원화학 | 고품질 사과 생산을 위한 특이적 적엽 기능성 액상 발효 비료 |
-
0
- BE BE538246D patent/BE538246A/xx unknown
-
1955
- 1955-05-18 CH CH344592D patent/CH344592A/de unknown
- 1955-05-20 GB GB14578/55A patent/GB785332A/en not_active Expired
- 1955-05-20 FR FR1131562D patent/FR1131562A/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20170077508A (ko) * | 2015-12-28 | 2017-07-06 | 주식회사 대원화학 | 고품질 사과 생산을 위한 특이적 적엽 기능성 액상 발효 비료 |
Also Published As
| Publication number | Publication date |
|---|---|
| CH344592A (de) | 1960-02-15 |
| FR1131562A (fr) | 1957-02-25 |
| BE538246A (th) | 1900-01-01 |
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