Cas 182265-88-9,(2R,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol

182265-88-9

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Basic information

Product Name: (2R,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol
Synonyms: (2R,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol
CAS NO:182265-88-9
Molecular Formula:
Molecular Weight: 686.961
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: (2R,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol(182265-88-9)
EPA Substance Registry System: (2R,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol(182265-88-9)

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: 182265-88-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 182265-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 182265-88:
(8*1)+(7*8)+(6*2)+(5*2)+(4*6)+(3*5)+(2*8)+(1*8)=149
149 % 10 = 9
So 182265-88-9 is a valid CAS Registry Number.

182265-88-9Upstream product

18162-48-6 tert-butyldimethylsilyl chloride

182265-88-9Downstream Products

182265-87-8 (2R,3S,4R,5R,6R)-3,4,5,7-Tetrakis-benzyloxy-heptane-1,2,6-triol

182265-88-9Relevant academic research and scientific papers

Chemical synthesis of β-homonojirimycin, of its N-butyl derivative, and of 'methyl homoazacellobioside'

Saavedra,Martin

, p. 6987 - 6993 (1996)

β-Homonojirimycin (2) was prepared by the highly stereoselective double reductive amination of a 2,6-heptodiulose derivative (6 or 13) using ammonium formate and NaBH3CN. The process was unsuccessful with primary amines. The synthesis of N-buty

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