Cas 1315510-28-1,dimethyl 2,2'-di-(3-chlorophenyl)-bis-5,5'-thiazole-4,4'-dicarboxylate

1315510-28-1

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Basic information

Product Name: dimethyl 2,2'-di-(3-chlorophenyl)-bis-5,5'-thiazole-4,4'-dicarboxylate
Synonyms: dimethyl 2,2'-di-(3-chlorophenyl)-bis-5,5'-thiazole-4,4'-dicarboxylate
CAS NO:1315510-28-1
Molecular Formula:
Molecular Weight: 505.402
EINECS: N/A
Product Categories: N/A
Mol File: 1315510-28-1.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: dimethyl 2,2'-di-(3-chlorophenyl)-bis-5,5'-thiazole-4,4'-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 2,2'-di-(3-chlorophenyl)-bis-5,5'-thiazole-4,4'-dicarboxylate(1315510-28-1)
EPA Substance Registry System: dimethyl 2,2'-di-(3-chlorophenyl)-bis-5,5'-thiazole-4,4'-dicarboxylate(1315510-28-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1315510-28-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1315510-28-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1315510-28:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*1)+(3*0)+(2*2)+(1*8)=111
111 % 10 = 1
So 1315510-28-1 is a valid CAS Registry Number.

1315510-28-1Upstream product

1315510-12-3 C₁₁H₈ClNO₂S

1315510-28-1Downstream Products

1315510-28-1Relevant articles and documents

Efficient palladium(II)-catalyzed homocoupling of thiazole-4-carboxylic or oxazole-4-carboxylic derivatives

Li, Ziyuan,Wang, Yiyun,Huang, Yue,Tang, Changhua,Xu, Jinyi,Wu, Xiaoming,Yao, Hequan

supporting information; experimental part, p. 5550 - 5555 (2011/08/06)

An efficient Pd(OAc)2-catalyzed homocoupling of thiazole-4-carboxylic or oxazole-4-carboxylic derivatives is described. It represents a facile and practical methodology to prepare bis-5,5′-thiazole (oxazole)-4,4′-dicarboxylic derivatives in goo

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