Cas 172096-98-9,(R)-4-Benzylsulfanylmethyl-5-oxo-oxazolidine-3-carboxylic acid tert-butyl ester

172096-98-9

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Basic information

Product Name: (R)-4-Benzylsulfanylmethyl-5-oxo-oxazolidine-3-carboxylic acid tert-butyl ester
Synonyms: (R)-4-Benzylsulfanylmethyl-5-oxo-oxazolidine-3-carboxylic acid tert-butyl ester
CAS NO:172096-98-9
Molecular Formula:
Molecular Weight: 323.413
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: (R)-4-Benzylsulfanylmethyl-5-oxo-oxazolidine-3-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-Benzylsulfanylmethyl-5-oxo-oxazolidine-3-carboxylic acid tert-butyl ester(172096-98-9)
EPA Substance Registry System: (R)-4-Benzylsulfanylmethyl-5-oxo-oxazolidine-3-carboxylic acid tert-butyl ester(172096-98-9)

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: 172096-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 172096-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,0,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 172096-98:
(8*1)+(7*7)+(6*2)+(5*0)+(4*9)+(3*6)+(2*9)+(1*8)=149
149 % 10 = 9
So 172096-98-9 is a valid CAS Registry Number.

172096-98-9Upstream product

172096-98-9Downstream Products

172096-98-9Relevant academic research and scientific papers

Reaction of (Trifluoromethyl)trimethylsilane with Oxazolidin-5-ones: Synthesis of Peptidic and Nonpeptidic Trifluoromethyl Ketones

Walter, Magnus W.,Adlington, Robert M.,Baldwin, Jack E.,Schofield, Christopher J.

, p. 5179 - 5192 (2007/10/03)

(Trifluoromethyl)trimethylsilane (TMS-CF3, the Ruppert Reagent) reacts with a variety of amino acid derived N-substituted oxazolidin-5-ones in excellent yields. Mild acid hydrolysis of adducts with electron-releasing substituents at C-2 affords

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