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1826-21-7

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1826-21-7 Usage

General Description

4-(4-Methoxy-phenyl)-thiazole is a chemical compound that belongs to the thiazole class of compounds. It is a heterocyclic organic compound containing a five-membered ring with sulfur and nitrogen atoms. 4-(4-METHOXY-PHENYL)-THIAZOLE has a molecular formula of C11H9NOS and a molecular weight of 211.27 g/mol. It is commonly used as a building block in the synthesis of various pharmaceutical, agrochemical, and material science products. Its structure and properties make it suitable for use in the development of novel drugs and other bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1826-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1826-21:
(6*1)+(5*8)+(4*2)+(3*6)+(2*2)+(1*1)=77
77 % 10 = 7
So 1826-21-7 is a valid CAS Registry Number.

1826-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methoxyphenyl)-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 4-<4-Methoxy-phenyl>-thiazol

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:1826-21-7 SDS

1826-21-7Relevant articles and documents

Programmed synthesis of arylthiazoles through sequential C-H couplings

Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro

, p. 123 - 135 (2014/01/06)

A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2

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