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103789-67-9

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103789-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103789-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,8 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103789-67:
(8*1)+(7*0)+(6*3)+(5*7)+(4*8)+(3*9)+(2*6)+(1*7)=139
139 % 10 = 9
So 103789-67-9 is a valid CAS Registry Number.

103789-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((2-phenylthiazol-4-yl)methoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(2-phenyl-thiazol-4-ylmethoxy)-benzaldehyde

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:103789-67-9 SDS

103789-67-9Relevant articles and documents

Tromethamine organocatalyzed efficient tandem-multicomponent synthesis of new thiazolyl-4-thiazolidinones in aqueous medium

Bhosle, Manisha R.,Kharote, Sayali A.,Bondle, Giribala M.,Mali, Jyotirling R.

, p. 1286 - 1300 (2019)

The catalytic potential of tris(hydroxymethyl)aminomethane (Tromethamine) has been assessed for the one pot three component tandem reaction involving a thiazolylmethoxy phenyl/aromatic carboxaldehyde, substituted amines and thioglycolic acid to form new t

An efficient synthesis of new pyrazolines and isoxazolines bearing thiazolyl and etheral pharmacophores

Bhosle, Manisha R.,Mali, Jyotirling R.,Pratap, Umesh R.,Mane, Ramrao A.

experimental part, p. 2012 - 2016 (2012/07/30)

A convenient synthetic route has been developed to synthesize 5-(4-((2-phenylthiazol-4-yl) methoxy)phenyl)-3-(4-sustituted phenyl)pyrazolines (5a-f) and 5-(4-((2-phenylthiazol-4-yl)methoxy)phenyl)-3-(4-substituted phenyl)isoxazolines (6a-f) starting from

PROCESS FOR PRODUCTION OF PYRAZOLE COMPOUNDS

-

Page 17, (2010/02/07)

As a method capable of conveniently producing a pyrazole compound in a high yield, which is useful as a synthetic intermediate for a pharmaceutical agent such as a therapeutic agent for diabetes and the like, a production method of a compound represented

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