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氟磺胺草醚

CAS 72178-02-0C15H10ClF3N2O6SMW 438.8

氟磺胺草醚(CAS 72178-02-0):分子式 C15H10ClF3N2O6S、分子量 438.8。

产品概览

CAS号72178-02-0
分子式C15H10ClF3N2O6S
分子量438.8
熔点220 °C
LogP2.9
应用领域Uses: Used as post-emergence herbicide for control of broad-leaved weeds in soy beans and other legumes、[Merck Index]、Farming (Pesticides) [Category: Industry]、For fomesafen sodium (USEPA、OPP Pesticide Code: 123802) ACTIVE products with label matches.、SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses.、Fomesafen sodium、Postemergence herbicide、over the top、on soybeans、Field experiments were conducted from 1991 to 1993 to evaluate eclipta、Eclipta prostrate L.、control and peanut、Arachis hypogaea L.、response to herbicide treatments. Formesafen (5-(2-chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide) applied at cracking was the only preemergence-applied herbicide which provided season-long control (>84%). Herbicides applied postemergence were more effective when the eclipta was less than 5 cm in height. Minor peanut injury was observed at the early season rating from several herbicides、however、all injury had disappeared by the late season rating. Eclipta control did not consistently improve peanut pod yield.、Methods of Manufacturing: Fomesafen is manufactured by reaction of 2-chloro-4-trifluoromethylphenolate with 4-chloro-N-methylsulfonyl-2-nitrobenzamide.、Acifluorfen + ammonia + methanesulfonyl chloride (amide formation、sulfonamide formation).、Formulations、Preparations: Aqueous concentration、liquid concentration.、Premix Partners: S-Metolachlor、Fenoxaprop-P-ethyl、Fluazifop-P-butyl、Glyphosate.、Basagran Herbicide (BASF Corporation) Sodium bentazon 44%、Formesafen sodium、Basagran M-60 Herbicide (BASF Corporation) MCPA、dimethylamine salt 6.2%、Sodium bentazon 37%、For more Formulations、Preparations (Complete) data for FOMESAFEN (12 total)、please visit the HSDB record page.、Consumption Patterns: In 1989、the national usage of formesafen was 227、000 lbs AI、year in U.S. agriculture.、General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies fomesafen (technical grade) as Class II: moderately hazardous、Main Use: herbicide.、Fomesafen was used on the following crops during the 1990 to 1993 crop years (from federal and state pesticide use surveys)、by crop (State、% of crop acreage treated based on estimates of the crop's 1992 planted acreage): green beans (AR、70%、IL、50%) and soybeans (AL、10%、AR、13%、FL、2%、GA、IN、KY、16%、LA、15%、MI、3%、MS、MO、NC、6%、OH、SC、and TN、9%).

应用领域

登记用途:Uses: Used as post-emergence herbicide for control of broad-leaved weeds in soy beans and other legumes、[Merck Index]、Farming (Pesticides) [Category: Industry]、For fomesafen sodium (USEPA、OPP Pesticide Code: 123802) ACTIVE products with label matches.、SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses.、Fomesafen sodium、Postemergence herbicide、over the top、on soybeans、Field experiments were conducted from 1991 to 1993 to evaluate eclipta、Eclipta prostrate L.、control and peanut、Arachis hypogaea L.、response to herbicide treatments. Formesafen (5-(2-chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide) applied at cracking was the only preemergence-applied herbicide which provided season-long control (>84%). Herbicides applied postemergence were more effective when the eclipta was less than 5 cm in height. Minor peanut injury was observed at the early season rating from several herbicides、however、all injury had disappeared by the late season rating. Eclipta control did not consistently improve peanut pod yield.、Methods of Manufacturing: Fomesafen is manufactured by reaction of 2-chloro-4-trifluoromethylphenolate with 4-chloro-N-methylsulfonyl-2-nitrobenzamide.、Acifluorfen + ammonia + methanesulfonyl chloride (amide formation、sulfonamide formation).、Formulations、Preparations: Aqueous concentration、liquid concentration.、Premix Partners: S-Metolachlor、Fenoxaprop-P-ethyl、Fluazifop-P-butyl、Glyphosate.、Basagran Herbicide (BASF Corporation) Sodium bentazon 44%、Formesafen sodium、Basagran M-60 Herbicide (BASF Corporation) MCPA、dimethylamine salt 6.2%、Sodium bentazon 37%、For more Formulations、Preparations (Complete) data for FOMESAFEN (12 total)、please visit the HSDB record page.、Consumption Patterns: In 1989、the national usage of formesafen was 227、000 lbs AI、year in U.S. agriculture.、General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies fomesafen (technical grade) as Class II: moderately hazardous、Main Use: herbicide.、Fomesafen was used on the following crops during the 1990 to 1993 crop years (from federal and state pesticide use surveys)、by crop (State、% of crop acreage treated based on estimates of the crop's 1992 planted acreage): green beans (AR、70%、IL、50%) and soybeans (AL、10%、AR、13%、FL、2%、GA、IN、KY、16%、LA、15%、MI、3%、MS、MO、NC、6%、OH、SC、and TN、9%).。

技术档案

这个产品是什么

氟磺胺草醚 是一种化工化合物,登记 CAS 号为 72178-02-0,分子式 C15H10ClF3N2O6S(分子量 438.8)。

识别信息

登记 CAS 号:72178-02-0

其分子式 C15H10ClF3N2O6S 由 15 个碳、10 个氢、1 个氯、3 个氟、2 个氮、6 个氧、1 个硫 组成。

别名/同义词:氟磺胺草醚 · Fomesafen

常见问题

氟磺胺草醚 的 CAS 号是多少?

氟磺胺草醚 的 CAS 登记号为 72178-02-0。

氟磺胺草醚 的分子式与分子量是多少?

分子式 C15H10ClF3N2O6S,分子量 438.8。

氟磺胺草醚 还有哪些别名?

别名/同义词:氟磺胺草醚、Fomesafen。

氟磺胺草醚 的登记用途是什么?

登记用途:Uses: Used as post-emergence herbicide for control of broad-leaved weeds in soy beans and other legumes、[Merck Index]、Farming (Pesticides) [Category: Industry]、For fomesafen sodium (USEPA、OPP Pesticide Code: 123802) ACTIVE products with label matches.、SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses.、Fomesafen sodium、Postemergence herbicide、over the top、on soybeans、Field experiments were conducted from 1991 to 1993 to evaluate eclipta、Eclipta prostrate L.、control and peanut、Arachis hypogaea L.、response to herbicide treatments. Formesafen (5-(2-chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide) applied at cracking was the only preemergence-applied herbicide which provided season-long control (>84%). Herbicides applied postemergence were more effective when the eclipta was less than 5 cm in height. Minor peanut injury was observed at the early season rating from several herbicides、however、all injury had disappeared by the late season rating. Eclipta control did not consistently improve peanut pod yield.、Methods of Manufacturing: Fomesafen is manufactured by reaction of 2-chloro-4-trifluoromethylphenolate with 4-chloro-N-methylsulfonyl-2-nitrobenzamide.、Acifluorfen + ammonia + methanesulfonyl chloride (amide formation、sulfonamide formation).、Formulations、Preparations: Aqueous concentration、liquid concentration.、Premix Partners: S-Metolachlor、Fenoxaprop-P-ethyl、Fluazifop-P-butyl、Glyphosate.、Basagran Herbicide (BASF Corporation) Sodium bentazon 44%、Formesafen sodium、Basagran M-60 Herbicide (BASF Corporation) MCPA、dimethylamine salt 6.2%、Sodium bentazon 37%、For more Formulations、Preparations (Complete) data for FOMESAFEN (12 total)、please visit the HSDB record page.、Consumption Patterns: In 1989、the national usage of formesafen was 227、000 lbs AI、year in U.S. agriculture.、General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies fomesafen (technical grade) as Class II: moderately hazardous、Main Use: herbicide.、Fomesafen was used on the following crops during the 1990 to 1993 crop years (from federal and state pesticide use surveys)、by crop (State、% of crop acreage treated based on estimates of the crop's 1992 planted acreage): green beans (AR、70%、IL、50%) and soybeans (AL、10%、AR、13%、FL、2%、GA、IN、KY、16%、LA、15%、MI、3%、MS、MO、NC、6%、OH、SC、and TN、9%).。

PubChem 公开数据

氟磺胺草醚(CAS 72178-02-0)的独立参考数据,整理自公开化学数据库。

各数据库的登记标识

CAS 号72178-02-0
PubChem CID51556
分子式C15H10ClF3N2O6S
IUPAC 名称5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-methylsulfonyl-2-nitrobenzamide
UNII(FDA)M0A3U4CDTF

计算分子描述符

Molecular Weight438.8
XLogP32.4
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count9
Rotatable Bond Count4
Exact Mass437.9900194
Monoisotopic Mass437.9900194
Topological Polar Surface Area127
Heavy Atom Count28

在册的理化数值

Melting Point220 °C
SolubilityIn water, 50 mg/L at 20 °C
Density1.28 g/cu cm at 20 °C
Vapor Pressure0.00000075 [mmHg]
Vapor Pressure<4X10-3 mPa /<3.0X10-8 mm Hg/ at 20 °C
LogP2.9
Dissociation ConstantspKa = 2.83

同义词与商品名

Fomesafen; 72178-02-0; Fomesafene; 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide; DTXSID7024112; M0A3U4CDTF; PP021; 5-(2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-N-mesyl-2-nitrobenzamide; 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide; DTXCID704112; CHEBI:81925; BENZAMIDE, 5-(2-CHLORO-4-(TRIFLUOROMETHYL)PHENOXY)-N-(METHYLSULFONYL)-2-NITRO-; 5-(2-chloro-4-(trifluoromethyl)-phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide; RefChem:141141; Reflex; 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-methylsulfonyl-2-nitrobenzamide

GHS 危害分类

已通报的危害声明H302, H332 (49.1%), H312 (17.5%), H400 (13.2%), H410 (13.2%)

公开数据库对它的描述

氟磺胺草醚 · CAS 72178-02-0 · C15H10ClF3N2O6S. UNII M0A3U4CDTF. Melting Point: 220 °C; Solubility: In water, 50 mg/L at 20 °C; Density: 1.28 g/cu cm at 20 °C.

数据来源:PubChem / Wikidata;与随货 COA 不一致时以 COA 为准。

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