Cas 97459-76-2,2-(4-Chloro-phenyl)-3-methyl-thiobutyric acid S-((R)-3-methyl-oxazolidin-4-ylmethyl) ester

97459-76-2

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Basic information

Product Name: 2-(4-Chloro-phenyl)-3-methyl-thiobutyric acid S-((R)-3-methyl-oxazolidin-4-ylmethyl) ester
Synonyms:
CAS NO:97459-76-2
Molecular Formula:
Molecular Weight: 327.875
EINECS: N/A
Product Categories: N/A

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: 2-(4-Chloro-phenyl)-3-methyl-thiobutyric acid S-((R)-3-methyl-oxazolidin-4-ylmethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-Chloro-phenyl)-3-methyl-thiobutyric acid S-((R)-3-methyl-oxazolidin-4-ylmethyl) ester(97459-76-2)
EPA Substance Registry System: 2-(4-Chloro-phenyl)-3-methyl-thiobutyric acid S-((R)-3-methyl-oxazolidin-4-ylmethyl) ester(97459-76-2)

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: 97459-76-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97459-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,5 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97459-76:
(7*9)+(6*7)+(5*4)+(4*5)+(3*9)+(2*7)+(1*6)=192
192 % 10 = 2
So 97459-76-2 is a valid CAS Registry Number.

97459-76-2Upstream product

97459-76-2Downstream Products

97459-76-2Relevant academic research and scientific papers

NOVEL RING TRANSFORMATION OF THIAZOLIDINE TO OXAZOLIDINE: ACYL HALIDE-PROMOTED INTRAMOLECULAR REARRANGEMENT OF 4(R)-HYDROXYMETHYL-3-METHYL-1,3-THIAZOLIDINE

Ando, Wataru,Takata, Toshikazu,Huang, Liren,Tamura, Yoshiharu

, p. 869 - 872 (1985)

An interesting transformation occurs during acylation of 4(R)-hydroxymethyl-3-methyl-1,3-thiazolidine when 4(R)-acylthiomethyl-3-methyl 1,3-oxazolidines are yielded: the reaction competing with O-acylation is controlled by the bulkiness of the acyl group.

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