Welcome to LookChem.com Sign In|Join Free

CAS

  • or

147150-35-4

Post Buying Request

147150-35-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Benzoic acid,3-chloro-2-[[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)sulfonyl]amino]-,methyl ester 147150-35-4

    Cas No: 147150-35-4

  • No Data

  • 1 Kilogram

  • 10000 Metric Ton/Month

  • Shanghai Upbio Tech Co.,Ltd
  • Contact Supplier

147150-35-4 Usage

Definition

ChEBI: The methyl ester of cloransulam. An inhibitor of acetohydroxyacid synthase (AHAS), it prevents the synthesis of amino acids in plants and is used as a herbicide for the control of post-emergence control of broad-leaved weeds in soybeans. It is not approved for use within the European Area.

Metabolic pathway

When 14C-cloransulam methyl is incubated with soils, the degradation proceeds via the hydrolysis of the ester group and O-de-ethylation on the triazolopyrimidine ring to yield the three identified metabolites, cloransulam, 5-hydroxycloransulam methyl, and 5-hydroxycloransulam. These metabolites are significantly less phytotoxic than the parent herbicide.

Check Digit Verification of cas no

The CAS Registry Mumber 147150-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147150-35:
(8*1)+(7*4)+(6*7)+(5*1)+(4*5)+(3*0)+(2*3)+(1*5)=114
114 % 10 = 4
So 147150-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H13ClFN5O5S/c1-3-27-15-18-10(17)7-11-19-14(20-22(11)15)28(24,25)21-12-8(13(23)26-2)5-4-6-9(12)16/h4-7,21H,3H2,1-2H3

147150-35-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cloransulam-methyl

1.2 Other means of identification

Product number -
Other names methyl 3-chloro-2-[[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)sulfonyl]amino]benzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:147150-35-4 SDS

147150-35-4Synthetic route

2-chlorosulfonyl-7-fluoro-5-ethoxy[1,2,4]triazolo[1,5-c]-pyrimidine
147150-77-4

2-chlorosulfonyl-7-fluoro-5-ethoxy[1,2,4]triazolo[1,5-c]-pyrimidine

methyl 3-chloroanthranilate
77820-58-7

methyl 3-chloroanthranilate

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide
147150-35-4

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide

Conditions
ConditionsYield
With pyridine; S,S-dimethyl-N-(2-methoxycarbonyl-6-chlorophenyl)sulfilimine In dichloromethane
With pyridine; S,S-dimethyl-N-(2-methoxycarbonyl-6-chlorophenyl)sulfilimine In dichloromethane
2-(trimethylsilyl)ethyl N-(tert-butoxycarbonyl)-L-cysteinate
172694-17-6

2-(trimethylsilyl)ethyl N-(tert-butoxycarbonyl)-L-cysteinate

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide
147150-35-4

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide

2-{7-[(R)-2-tert-Butoxycarbonylamino-2-(2-trimethylsilanyl-ethoxycarbonyl)-ethylsulfanyl]-5-ethoxy-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonylamino}-3-chloro-benzoic acid methyl ester
172694-18-7

2-{7-[(R)-2-tert-Butoxycarbonylamino-2-(2-trimethylsilanyl-ethoxycarbonyl)-ethylsulfanyl]-5-ethoxy-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonylamino}-3-chloro-benzoic acid methyl ester

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide for 4h; Ambient temperature;90%
TMSEO-β-ala-N-t-Boc-(R)-cys-SH
172694-28-9

TMSEO-β-ala-N-t-Boc-(R)-cys-SH

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide
147150-35-4

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide

2-(7-{(R)-2-tert-Butoxycarbonylamino-2-[2-(2-trimethylsilanyl-ethoxycarbonyl)-ethylcarbamoyl]-ethylsulfanyl}-5-ethoxy-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonylamino)-3-chloro-benzoic acid methyl ester
172694-29-0

2-(7-{(R)-2-tert-Butoxycarbonylamino-2-[2-(2-trimethylsilanyl-ethoxycarbonyl)-ethylcarbamoyl]-ethylsulfanyl}-5-ethoxy-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonylamino)-3-chloro-benzoic acid methyl ester

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide for 4.5h; Ambient temperature;48%
N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide
147150-35-4

N-(2-methoxycarbonyl-6-chlorophenyl)-7-fluoro-5-ethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonamide

diazomethyl-trimethyl-silane
18107-18-1

diazomethyl-trimethyl-silane

3-Chloro-2-[(5-ethoxy-7-fluoro-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonyl)-methyl-amino]-benzoic acid methyl ester

3-Chloro-2-[(5-ethoxy-7-fluoro-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonyl)-methyl-amino]-benzoic acid methyl ester

Conditions
ConditionsYield
With phosphoric acid In hexane; acetone for 0.5h; Ambient temperature;

147150-35-4Relevant articles and documents

N-ARYLSULFILIMINE COMPOUNDS AND THEIR USE AS CATALYSTS IN THE PREPARATION OF N-ARYLARYLSULFONAMIDE COMPOUNDS

-

, (2008/06/13)

N-arylsulfilimine compounds, such as S,S-dimethyl-N-(2,6-dichlorophenyl)sulfilimine, were prepared and found to catalyze the reaction of aromatic sulfonyl chloride compounds, such as 2-chlorosulfonyl-7-fluoro-5-ethoxy[1,2,4]triazolo[1,5-c]pyrimidine, with aromatic amine compounds, such as 2,6-dichloroaniline, to form N-arylarylsulfonamide compounds, such as N-(2,6-dichlorophenyl)-7-fluoro-5-ethoxy[1,2,4]triazolo[1,5-c]-pyrimidine-2-sulfonamide. The aryl moiety of the N-arylsulfilimine catalyst and the aryl moiety of the aromatic amine compound were generally chosen to be identical.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 147150-35-4