Cas 1263098-05-0,(R,S)-ethyl-2-(4-(pyridin-4-yl)-phenyl)-thiazolidine-4-(R)-carboxylate

1263098-05-0

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Basic information

Product Name: (R,S)-ethyl-2-(4-(pyridin-4-yl)-phenyl)-thiazolidine-4-(R)-carboxylate
Synonyms: (R,S)-ethyl-2-(4-(pyridin-4-yl)-phenyl)-thiazolidine-4-(R)-carboxylate
CAS NO:1263098-05-0
Molecular Formula:
Molecular Weight: 314.408
EINECS: N/A
Product Categories: N/A
Mol File: 1263098-05-0.mol
Article Data: 2

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: (R,S)-ethyl-2-(4-(pyridin-4-yl)-phenyl)-thiazolidine-4-(R)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R,S)-ethyl-2-(4-(pyridin-4-yl)-phenyl)-thiazolidine-4-(R)-carboxylate(1263098-05-0)
EPA Substance Registry System: (R,S)-ethyl-2-(4-(pyridin-4-yl)-phenyl)-thiazolidine-4-(R)-carboxylate(1263098-05-0)

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: 1263098-05-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1263098-05-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,0,9 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1263098-05:
(9*1)+(8*2)+(7*6)+(6*3)+(5*0)+(4*9)+(3*8)+(2*0)+(1*5)=150
150 % 10 = 0
So 1263098-05-0 is a valid CAS Registry Number.

1263098-05-0Upstream product

1263098-05-0Downstream Products

1263098-09-4 2-[4-(pyridin-4-yl)phenyl]-thiazole-4-carboxylic acid

1263098-05-0Relevant articles and documents

Design and synthesis of thiazole and thiazolidine metallo-supramolecular networks

Di Credico, Barbara,Gonsalvi, Luca,Peruzzini, Maurizio,Reginato, Gianna,Rossin, Andrea

, p. 1312 - 1315 (2011)

A mild and selective procedure for the synthesis of 4-carboxy thiazoles and thiazolidines starting from naturally occurring cysteine by condensation with aldehydes is described. The optimized procedure, taking advantage of the positive effect of microwave

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