Cas 366806-80-6,4-Thiazolidinecarboxylicacid,2-ethyl-,1-methylethylester,(2R,4R)-(9CI)

366806-80-6

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Basic information

Product Name: 4-Thiazolidinecarboxylicacid,2-ethyl-,1-methylethylester,(2R,4R)-(9CI)
Synonyms: 4-Thiazolidinecarboxylicacid,2-ethyl-,1-methylethylester,(2R,4R)-(9CI)
CAS NO:366806-80-6
Molecular Formula: C9H17NO2S
Molecular Weight: 203.3
EINECS: N/A
Product Categories: ETHYL
Mol File: 366806-80-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 287.7±35.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.054±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 7.02±0.60(Predicted)
CAS DataBase Reference: 4-Thiazolidinecarboxylicacid,2-ethyl-,1-methylethylester,(2R,4R)-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 4-Thiazolidinecarboxylicacid,2-ethyl-,1-methylethylester,(2R,4R)-(9CI)(366806-80-6)
EPA Substance Registry System: 4-Thiazolidinecarboxylicacid,2-ethyl-,1-methylethylester,(2R,4R)-(9CI)(366806-80-6)

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: 366806-80-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 366806-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,6,8,0 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 366806-80:
(8*3)+(7*6)+(6*6)+(5*8)+(4*0)+(3*6)+(2*8)+(1*0)=176
176 % 10 = 6
So 366806-80-6 is a valid CAS Registry Number.

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366806-80-6Relevant academic research and scientific papers

Asymmetric synthesis of 2-alkyl-3-thiazoline carboxylates: Stereochemistry of the MnO2-mediated oxidation of cis- and trans-2-alkyl-thiazolidine-(4R)-carboxylates

Fernandez, Xavier,Duach, Elisabet

, p. 1279 - 1286 (2007/10/03)

The asymmetric synthesis of a series of 3-thiazoline carboxylates, 2, was effected by MnO2 oxidation of the corresponding cis/trans thiazolidines, 1. The stereochemistry of the oxidation reaction was studied using NMR and chiral GC analyses. Compounds 2 were obtained with enantiomeric excesses (e.e.s) in the range of 40-100%.

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