Cas 1009867-72-4,(1R,2R)-2-amino-(N-benzyloxycarbonyl)-1,3-O-di(tert-butyldimethylsilyl)-1-phenylpropane-1,3-diol

1009867-72-4

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Basic information

Product Name: (1R,2R)-2-amino-(N-benzyloxycarbonyl)-1,3-O-di(tert-butyldimethylsilyl)-1-phenylpropane-1,3-diol
Synonyms: (1R,2R)-2-amino-(N-benzyloxycarbonyl)-1,3-O-di(tert-butyldimethylsilyl)-1-phenylpropane-1,3-diol
CAS NO:1009867-72-4
Molecular Formula:
Molecular Weight: 529.867
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: (1R,2R)-2-amino-(N-benzyloxycarbonyl)-1,3-O-di(tert-butyldimethylsilyl)-1-phenylpropane-1,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R)-2-amino-(N-benzyloxycarbonyl)-1,3-O-di(tert-butyldimethylsilyl)-1-phenylpropane-1,3-diol(1009867-72-4)
EPA Substance Registry System: (1R,2R)-2-amino-(N-benzyloxycarbonyl)-1,3-O-di(tert-butyldimethylsilyl)-1-phenylpropane-1,3-diol(1009867-72-4)

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: 1009867-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1009867-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,8,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1009867-72:
(9*1)+(8*0)+(7*0)+(6*9)+(5*8)+(4*6)+(3*7)+(2*7)+(1*2)=164
164 % 10 = 4
So 1009867-72-4 is a valid CAS Registry Number.

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1009867-72-4Relevant academic research and scientific papers

Syntheses of 1,2-amino alcohols and their applications for oxazaborolidine catalyzed enantioselective reduction of aromatic ketones

Vatmurge, Namdev S.,Hazra, Braja G.,Pore, Vandana S.

, p. 196 - 204 (2008/02/11)

Six new chiral 1,2-amino alcohol derivatives have been synthesized starting from (1R,2R)-2-amino-1-phenylpropane-1,3-diol. Asymmetric reduction of aryl ketones with in-situ generated oxazaborolidine from these amino alcohol derivatives and BH3?

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