Cas 339343-22-5,3-ACETYL-2-(4-METHOXY-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID

339343-22-5

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Basic information

Product Name: 3-ACETYL-2-(4-METHOXY-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID
Synonyms: 3-ACETYL-2-(4-METHOXY-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID;(2R,4R)-3-acetyl-2-(4-methoxyphenyl)-1,3-thiazolidine-4-carboxylic acid;4-thiazolidinecarboxylic acid, 3-acetyl-2-(4-methoxyphenyl;(2R,4R)-3-acetyl-2-(4-methoxyphenyl)-4-thiazolidinecarboxylic acid;(2R,4R)-3-acetyl-2-(4-methoxyphenyl)thiazolidine-4-carboxylic acid;(2R,4R)-3-ethanoyl-2-(4-methoxyphenyl)-1,3-thiazolidine-4-carboxylic acid;MFCD13248707
CAS NO:339343-22-5
Molecular Formula: C13H15NO4S
Molecular Weight: 281.33
EINECS: N/A
Product Categories: N/A
Mol File: 339343-22-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-ACETYL-2-(4-METHOXY-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID(CAS DataBase Reference)
NIST Chemistry Reference: 3-ACETYL-2-(4-METHOXY-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID(339343-22-5)
EPA Substance Registry System: 3-ACETYL-2-(4-METHOXY-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID(339343-22-5)

Safety Data

Hazard Codes: Xi
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: IRRITANT
PackingGroup: N/A
Hazardous Substances Data: 339343-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 339343-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,3,4 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 339343-22:
(8*3)+(7*3)+(6*9)+(5*3)+(4*4)+(3*3)+(2*2)+(1*2)=145
145 % 10 = 5
So 339343-22-5 is a valid CAS Registry Number.

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339343-22-5Relevant articles and documents

Synthesis and Chiroptical Properties of N-Acetyl-2-aryl-4-thiazolidinecarboxylic Acids

Gyoergydeak, Zoltan,Kajtar-Peredy, Maria,Kajtar, Judit,Kajtar, Marton

, p. 927 - 934 (2007/10/02)

(4R)-2-Aryl-4-thiazolidinecarboxylic acids 3, derived from aromatic aldehydes 1 and L-cysteine (2), could be diastereoselectively converted into (2R,4R)- or (2S,4R)-N-acetyl-2-aryl-4-thiazolidinecarboxylic acids (4 and 5, resp.).The diastereomers can be d

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