Cas 852609-51-9,(S)-4-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

852609-51-9

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Basic information

Product Name: (S)-4-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
Synonyms: (S)-4-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
CAS NO:852609-51-9
Molecular Formula:
Molecular Weight: 469.696
EINECS: N/A
Product Categories: N/A
Mol File: 852609-51-9.mol
Article Data: 2

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-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester(852609-51-9)
EPA Substance Registry System: (S)-4-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester(852609-51-9)

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: 852609-51-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 852609-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,6,0 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 852609-51:
(8*8)+(7*5)+(6*2)+(5*6)+(4*0)+(3*9)+(2*5)+(1*1)=179
179 % 10 = 9
So 852609-51-9 is a valid CAS Registry Number.

852609-51-9Upstream product

852609-51-9Downstream Products

852609-51-9Relevant articles and documents

Chemoselective deprotection of cyclic N,O-aminals using catalytic bismuth(III) bromide in acetonitrile

Cong, Xin,Hu, Fang,Liu, Ke-Gang,Liao, Qing-Jiang,Yao, Zhu-Jun

, p. 4514 - 4516 (2005)

Cyclic N,O-aminals can be chemoselectively and efficiently deprotected using a catalytic amount of bismuth(III) bromide in acetonitrile at room temperature. This selectivity was also achieved in the presence of terminal O,O-acetal functionality. The susce

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