Cas 376369-15-2,4-[2-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-cyclopropyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid <i>tert</i>-butyl ester

376369-15-2

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Basic information

Product Name: 4-[2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopropyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
Synonyms: 4-[2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopropyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
CAS NO:376369-15-2
Molecular Formula:
Molecular Weight: 509.761
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: 4-[2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopropyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopropyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester(376369-15-2)
EPA Substance Registry System: 4-[2-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopropyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester(376369-15-2)

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: 376369-15-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 376369-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,6,3,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 376369-15:
(8*3)+(7*7)+(6*6)+(5*3)+(4*6)+(3*9)+(2*1)+(1*5)=182
182 % 10 = 2
So 376369-15-2 is a valid CAS Registry Number.

376369-15-2Upstream product

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376369-15-2Relevant academic research and scientific papers

A concise and efficient stereoselective synthesis of protected (2R,1′S,2′S)-2-(carboxycyclopropyl)glycine (D-CCG-I)

Mohapatra

, p. 1851 - 1852 (2007/10/03)

The stereoselective synthesis of protected D-carboxycyclo-propylglycine (D-CCG-I) was achieved, as an extension of Taguchi's protocol for Simmons-Smith cyclopropanation to a chiral, amino-containing allyl alcohol derivative, in 8 steps (40% overall yield)

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