Cas 596108-86-0,3-Oxazolidinecarboxylic acid, 5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethyl-4-(2-propen yl)-, 1,1-dimethylethyl ester, (4R,5R)-

596108-86-0

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Basic information

Product Name: 3-Oxazolidinecarboxylic acid, 5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethyl-4-(2-propen yl)-, 1,1-dimethylethyl ester, (4R,5R)-
Synonyms:
CAS NO:596108-86-0
Molecular Formula: C30H43NO4Si
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: 3-Oxazolidinecarboxylic acid, 5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethyl-4-(2-propen yl)-, 1,1-dimethylethyl ester, (4R,5R)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxazolidinecarboxylic acid, 5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethyl-4-(2-propen yl)-, 1,1-dimethylethyl ester, (4R,5R)-(596108-86-0)
EPA Substance Registry System: 3-Oxazolidinecarboxylic acid, 5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethyl-4-(2-propen yl)-, 1,1-dimethylethyl ester, (4R,5R)-(596108-86-0)

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: 596108-86-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 596108-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,1,0 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 596108-86:
(8*5)+(7*9)+(6*6)+(5*1)+(4*0)+(3*8)+(2*8)+(1*6)=190
190 % 10 = 0
So 596108-86-0 is a valid CAS Registry Number.

596108-86-0Upstream product

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596108-86-0Relevant academic research and scientific papers

New stereodivergent approach to 3-amino-2,3,6-trideoxysugars. Enantioselective synthesis of daunosamine, ristosamine, acosamine, and epi-daunosamine

Ginesta, Xavier,Pasto, Mireia,Pericas, Miquel A.,Riera, Antoni

, p. 3001 - 3004 (2007/10/03)

(Matrix presented) An enantioselective preparation of the four diastereomeric 3-amino-2,3,6-trideoxy-hexoses, key components of anthracycline antibiotics, has been developed. Sharpless catalytic asymmetric epoxidation of the (2E)-2,5-hexadien-1-ol, regios

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