Cas 1263098-07-2,(R,S)-ethyl-2-[4-(methoxycarbonyl)phenyl]-thiazolidine-4-(R)-carboxylate

1263098-07-2

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Basic information

Product Name: (R,S)-ethyl-2-[4-(methoxycarbonyl)phenyl]-thiazolidine-4-(R)-carboxylate
Synonyms: (R,S)-ethyl-2-[4-(methoxycarbonyl)phenyl]-thiazolidine-4-(R)-carboxylate
CAS NO:1263098-07-2
Molecular Formula:
Molecular Weight: 309.386
EINECS: N/A
Product Categories: N/A
Mol File: 1263098-07-2.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-(methoxycarbonyl)phenyl]-thiazolidine-4-(R)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R,S)-ethyl-2-[4-(methoxycarbonyl)phenyl]-thiazolidine-4-(R)-carboxylate(1263098-07-2)
EPA Substance Registry System: (R,S)-ethyl-2-[4-(methoxycarbonyl)phenyl]-thiazolidine-4-(R)-carboxylate(1263098-07-2)

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: 1263098-07-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1263098-07-2 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 1263098-07:
(9*1)+(8*2)+(7*6)+(6*3)+(5*0)+(4*9)+(3*8)+(2*0)+(1*7)=152
152 % 10 = 2
So 1263098-07-2 is a valid CAS Registry Number.

1263098-07-2Upstream product

1263098-07-2Downstream Products

1321497-20-4 C₁₃H₁₁NO₄S

1263098-07-2Relevant articles and documents

Selective synthesis of 2-substituted 4-carboxy oxazoles, thiazoles and thiazolidines from serine or cysteine amino acids

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

experimental part, p. 267 - 274 (2011/02/26)

The synthesis of new 4-carboxy oxazoles, thiazoles and thiazolidines by condensation of serine or cysteine with aldehydes or acids is described. Due to the optimization of a mild and selective procedure, which takes advantage of the positive effect of mic

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