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148934-66-1

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148934-66-1 Usage

General Description

Methyl 3-chloro-1-methyl-1H-pyrazole-4-carboxylate is a chemical compound with the molecular formula C6H7ClN2O2. It is a chlorinated derivative of pyrazole and is often used as an intermediate for the synthesis of pharmaceuticals and agrochemicals. Methyl 3-chloro-1-methyl-1H-pyrazole-4-carboxylate is known for its diverse biological activities, including antimicrobial, anti-inflammatory, and antifungal properties. It is commonly used in the production of pesticides and herbicides due to its ability to inhibit the growth of certain microorganisms and pests. Additionally, it has potential applications in the development of drugs for treating various diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 148934-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,3 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 148934-66:
(8*1)+(7*4)+(6*8)+(5*9)+(4*3)+(3*4)+(2*6)+(1*6)=171
171 % 10 = 1
So 148934-66-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2O2/c1-9-3-4(5(7)8-9)6(10)11-2/h3H,1-2H3

148934-66-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-chloro-1-methylpyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 3-chloro-1-methyl-1H-pyrazole-4-carboxylate

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:148934-66-1 SDS

148934-66-1Relevant articles and documents

Synthesis of Halosulfuron-methyl via Selective Chlorination at 3- and/or 5-Position of Pyrazole-4-carboxylates

Morimoto, Katsushi,Sato, Toshiaki,Yamamoto, Susumu,Takeuchi, Hiroshi

, p. 537 - 540 (2007/10/03)

Reactions of methyl pyrazole-4-carboxylates 4b-d with N-chlorosuccinimide under heating conditions without a solvent gave methyl 3,5-dichloro-1-methylpyrazole-4-carboxylate 4a in good yields. The reaction of 4a with sodium hydrosulfide led to a nucleophilic substitution on the 5-position regioselectively to afford methyl 3-chloro-1-methyl-5-mercaptopyrazole-4-carboxylate 6a, which was followed by oxidative chlorination and amination to obtain 3-chloro-1-methyl-5-sulfamoylpyrazole-4-carboxylate 2a. Finally, the reaction of 2a with phenyl 4,6-dimethoxypyrimidin-2-yl carbamate 7 provided methyl 3-chloro-5-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-1-methylpyrazole-4- carboxylate (halosulfuron-methyl) 1a promising herbicide in corn.

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