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35550-13-1

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35550-13-1 Usage

Family

Thiadiazole

Amine group

Attached to the 5th carbon

Methyl groups

Two methyl groups attached to the 3rd nitrogen

Building block

In organic synthesis

Pharmaceutical production

Used in the production of pharmaceuticals

Agrochemicals

Used in the production of agrochemicals

Biological activity

Exhibits potential biological activity

Intermediate

Valuable intermediate for the development of new drugs

Role in coordination chemistry

Acts as a ligand, forming complexes with transition metals for various applications

Check Digit Verification of cas no

The CAS Registry Mumber 35550-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,5 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35550-13:
(7*3)+(6*5)+(5*5)+(4*5)+(3*0)+(2*1)+(1*3)=101
101 % 10 = 1
So 35550-13-1 is a valid CAS Registry Number.

35550-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,3-dimethyl-1,2,4-thiadiazol-5-amine

1.2 Other means of identification

Product number -
Other names 5-Methylamino-3-methyl-1,2,4-thiodiazol

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:35550-13-1 SDS

35550-13-1Downstream Products

35550-13-1Relevant articles and documents

Substituted 5-amino-1,2,4-thiadiazoles with pharmaceutical activity

-

, (2008/06/13)

Pharmaceutical compounds of the following formula are described: in which R1 is hydrogen, C1 4 alkyl, C1 4 alkoxy-C1 4 alkyl, hydroxy-C1 4 alkyl, optionally substituted phenyl, optionally substituted phenyl-C1 4 alkyl or a heterocycle selected from: where R3 is hydrogen, C1 4 alkyl, C1 4 alkoxy, nitro, halo, cyano, trifluoromethyl, carboxyl or -CONH2, and R4 is C1 4 alkyl; and R2 is hydrogen, C1 4 alkyl, phenyl or thienyl substituted with a carboxyl or C1 4 alkoxy-carbonyl group, an acyl group of the formula R5CO- where R5 is hydrogen, C1 4 alkyl, C1 4 alkoxy-C1 4 alkyl, halo C1 4 alkyl, C1 4 alkoxy, halo-C1 4 alkoxy, phenyl, phenyl-C1 4 alkyl, -NHC1 4 alkyl, -NH phenyl or where R6 is C1 4 alkyl, or a group of the formula -CH=C(COC1 4 alkoxy)2; or a salt thereof.

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