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3-Isothiazolecarboxamide,4-amino-N-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115106-39-3

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115106-39-3 Usage

Functional Groups

Isothiazole ring (containing nitrogen and sulfur)
Carboxamide group
Methylamine group (N-methyl substitution)

Application

Often used in the pharmaceutical industry

Utility

Serves as a building block for synthesizing various drugs

Structural Characteristics

Contains an amino group at the 4th position of the isothiazole ring
N-methyl substitution at the amino group

Modifiability

Structure allows for modifications, aiding in drug discovery and development

Pharmacological Interest

Potential biological activities
Pharmacological properties

Research Relevance

Draws interest from researchers and scientists in medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 115106-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,0 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115106-39:
(8*1)+(7*1)+(6*5)+(5*1)+(4*0)+(3*6)+(2*3)+(1*9)=83
83 % 10 = 3
So 115106-39-3 is a valid CAS Registry Number.

115106-39-3SDS

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 4-amino-N-methyl-1,2-thiazole-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-isothiazolecarboxamide,4-amino-n-methyl

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:115106-39-3 SDS

115106-39-3Downstream Products

115106-39-3Relevant academic research and scientific papers

A Novel Formation of 3,4-Disubstituted Isothiazoles from 5-Amino-6-methylpyrimidinones

Ueda, Taisei,Shibata, Yoshitugu,Kato, Yuzo,Sakakibara, Jinsaku

, p. 3917 - 3922 (2007/10/02)

3,4-Disubstituted isothiazoles (8a,b, 9a,b, 10, 11, 14a,b) were synthesized from 5-amino-6-methyl-4(3H)-pyrimidinone (1) or 1,3-disubstituted 5-amino-6-methyluracils (12a,b) via the formation of isothiazolopyrimidines (6, 13a,b) followed by the rea

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