Cas 1129725-34-3,tert-butyl (4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-chlorotetrahydro-2H-pyran-2-ylcarbamate

1129725-34-3

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Basic information

Product Name: tert-butyl (4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-chlorotetrahydro-2H-pyran-2-ylcarbamate
Synonyms: tert-butyl (4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-chlorotetrahydro-2H-pyran-2-ylcarbamate
CAS NO:1129725-34-3
Molecular Formula:
Molecular Weight: 568.11
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: tert-butyl (4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-chlorotetrahydro-2H-pyran-2-ylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-chlorotetrahydro-2H-pyran-2-ylcarbamate(1129725-34-3)
EPA Substance Registry System: tert-butyl (4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-chlorotetrahydro-2H-pyran-2-ylcarbamate(1129725-34-3)

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: 1129725-34-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1129725-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,9,7,2 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1129725-34:
(9*1)+(8*1)+(7*2)+(6*9)+(5*7)+(4*2)+(3*5)+(2*3)+(1*4)=153
153 % 10 = 3
So 1129725-34-3 is a valid CAS Registry Number.

1129725-34-3Upstream product

1129725-34-3Downstream Products

1129725-41-2 tert-butyl (4R,5S,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran-2-ylcarbamate

1129725-34-3Relevant academic research and scientific papers

Efficient and stereodivergent syntheses of D- and L-fagomines and their analogues

Kumari, Nitee,Reddy, B. Gopal,Vankar, Yashwant D.

, p. 160 - 169 (2009)

The syntheses of D- and L-fagomines 1, 4, 5 and 6 and their isomers from starting D-glycals have been achieved. The syntheses involve elaboration of common amino alcohol precursors obtained from 2-deoxy-1-amino sugar derivatives. The key steps in the synt

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