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120740-06-9

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120740-06-9 Usage

General Description

(2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine is a chemical compound that contains a thiazole ring with a chlorine atom and a methyl group attached to it. (2-Chloro-thiazol-5-ylMethyl)-Methyl-aMine also has an amine group, which consists of a nitrogen atom bonded to three hydrogen atoms. The presence of the chloro-thiazole and methyl groups makes this compound suitable for use in medicinal chemistry and pharmaceutical research as it can potentially act as a building block for the synthesis of biologically active molecules. Additionally, the amine group provides this compound with the ability to form important chemical reactions and participate in various biological processes within living organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 120740-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,4 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120740-06:
(8*1)+(7*2)+(6*0)+(5*7)+(4*4)+(3*0)+(2*0)+(1*6)=79
79 % 10 = 9
So 120740-06-9 is a valid CAS Registry Number.

120740-06-9SDS

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 1-(2-chloro-1,3-thiazol-5-yl)-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names (2-Chloro-thiazol-5-ylmethyl)-methyl-amine

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:120740-06-9 SDS

120740-06-9Downstream Products

120740-06-9Relevant articles and documents

Substituted benzisothiazole compound and application

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Paragraph 0148; 0150; 0153; 0154, (2018/03/24)

The invention discloses a substituted benzisothiazole compound. R1 is cyan, hydroxyl, C1-C4 alkyl, cyclopropyl, cyanomethyl, methoxyl, ethyoxyl, acetyl, trifluoroacetyl, C1-C4 alkoxycarbonyl and methylsulfonyl or ethylsulfonyl, R2 is independently selected from hydrogen, halogen, cyan, methyl, methoxyl, trifluoromethyl and trifluoromethoxyl or difluoromethoxyl, n is 1, 2, 3 or 4, m is 1 or 2, and J is replaced thiazole, isothiazole or pyridine. The compound has excellent activity and good plant tolerance and environmental safety under low concentration and can inhibit or destroy various pathogenic fungi and bacteria generated by plants or soil and kill various insect pests and mites, and sterilization and insecticidal spectrums of the compound are widened. According to the preparation method, used raw materials are economical and easy to get, and the preparation method is high in yield and low in synthesis process cost and has good sterilization activity and pest and mite killing activity.

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