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1235406-42-4

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1235406-42-4 Usage

General Description

Tert-butyl thiazol-4-ylcarbamate is a chemical compound with the molecular formula C9H16N2O2S. It is a carbamate derivative with a thiazole ring and a tert-butyl group attached to the nitrogen atom. tert-butyl thiazol-4-ylcarbamate is commonly used as a synthetic intermediate in the pharmaceutical industry for the production of various drugs and pharmaceuticals. It possesses potential biological activities and may have applications in medicinal and agricultural research. Tert-butyl thiazol-4-ylcarbamate is also used as a building block in organic synthesis for the preparation of diverse organic compounds. However, like any chemical compound, it should be handled with care and in accordance with proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 1235406-42-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,4,0 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1235406-42:
(9*1)+(8*2)+(7*3)+(6*5)+(5*4)+(4*0)+(3*6)+(2*4)+(1*2)=124
124 % 10 = 4
So 1235406-42-4 is a valid CAS Registry Number.

1235406-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl thiazol-4-ylcarbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-(1,3-thiazol-4-yl)carbamate

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:1235406-42-4 SDS

1235406-42-4Relevant articles and documents

Novel syntheses of variably substituted pyrrolo[2,3-d]thiazoles

Koolman, Hannes,Heinrich, Timo,Reggelin, Michael

scheme or table, p. 3152 - 3162 (2010/11/03)

Pyrrolo[2,3-d]thiazoles are conveniently derived from the corresponding o-aminoalkynylthiazoles via microwave assisted 5-endo-dig cyclization. Methylene-bridged substituents in the 6-position are directly obtained from 5-exo-Heck cyclization based on the

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