Cas 1235561-85-9,(2S,3R)-2-(N,N'-bis(benzyloxycarbonyl)hydrazino)-1,3-bis-(tert-butyldimethylsilyloxy)dodecane

1235561-85-9

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Basic information

Product Name: (2S,3R)-2-(N,N'-bis(benzyloxycarbonyl)hydrazino)-1,3-bis-(tert-butyldimethylsilyloxy)dodecane
Synonyms: (2S,3R)-2-(N,N'-bis(benzyloxycarbonyl)hydrazino)-1,3-bis-(tert-butyldimethylsilyloxy)dodecane
CAS NO:1235561-85-9
Molecular Formula:
Molecular Weight: 729.161
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: (2S,3R)-2-(N,N'-bis(benzyloxycarbonyl)hydrazino)-1,3-bis-(tert-butyldimethylsilyloxy)dodecane(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-2-(N,N'-bis(benzyloxycarbonyl)hydrazino)-1,3-bis-(tert-butyldimethylsilyloxy)dodecane(1235561-85-9)
EPA Substance Registry System: (2S,3R)-2-(N,N'-bis(benzyloxycarbonyl)hydrazino)-1,3-bis-(tert-butyldimethylsilyloxy)dodecane(1235561-85-9)

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: 1235561-85-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1235561-85-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,5,6 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1235561-85:
(9*1)+(8*2)+(7*3)+(6*5)+(5*5)+(4*6)+(3*1)+(2*8)+(1*5)=149
149 % 10 = 9
So 1235561-85-9 is a valid CAS Registry Number.

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1235561-85-9Relevant academic research and scientific papers

Asymmetric synthesis of sphinganine and clavaminol H

Ait-Youcef, Ramzi,Moreau, Xavier,Greck, Christine

, p. 5312 - 5315 (2010)

(Figure presented) An efficient enantioselective synthesis of sphinganine and clavaminol H is reported. These sphingoid-type bases were obtained from commercially available fatty acids using highly enantioselective Ru-catalyzed hydrogenation and organocatalytic electrophilic amination reactions to create the stereogenic centers.

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