Cas 143736-37-2,(S)-4-Cyclohexylmethyl-3-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-oxazolidin-2-one

143736-37-2

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Basic information

Product Name: (S)-4-Cyclohexylmethyl-3-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-oxazolidin-2-one
Synonyms:
CAS NO:143736-37-2
Molecular Formula:
Molecular Weight: 363.497
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: (S)-4-Cyclohexylmethyl-3-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-Cyclohexylmethyl-3-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-oxazolidin-2-one(143736-37-2)
EPA Substance Registry System: (S)-4-Cyclohexylmethyl-3-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-oxazolidin-2-one(143736-37-2)

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: 143736-37-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143736-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,3 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143736-37:
(8*1)+(7*4)+(6*3)+(5*7)+(4*3)+(3*6)+(2*3)+(1*7)=132
132 % 10 = 2
So 143736-37-2 is a valid CAS Registry Number.

143736-37-2Upstream product

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143736-37-2Relevant academic research and scientific papers

Practical Preparation of Chiral 4-Substituted 2-Oxazolidinones

Ishizuka, Tadao,Kimura, Koreichi,Ishibuchi, Seigo,Kunieda, Takehisa

, p. 991 - 994 (2007/10/02)

A versatile and practical route to both enantiomers of a wide variety of 4-substituted 2-oxazolidinones from the parent heterocycle is provided by regioselective substitutions via 4-methoxy derivative followed by chromatographic separation of the diastereomers derived from N-2-exo-methoxy-1-apocamphanecarbonylation.

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