Cas 880548-65-2,(2S,4S,5R)-1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)-2-hydroxymethyl-4-(tert-butyldiphenylsilyloxy)piperidine

880548-65-2

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Basic information

Product Name: (2S,4S,5R)-1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)-2-hydroxymethyl-4-(tert-butyldiphenylsilyloxy)piperidine
Synonyms: (2S,4S,5R)-1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)-2-hydroxymethyl-4-(tert-butyldiphenylsilyloxy)piperidine
CAS NO:880548-65-2
Molecular Formula:
Molecular Weight: 584.828
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,4S,5R)-1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)-2-hydroxymethyl-4-(tert-butyldiphenylsilyloxy)piperidine(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S,5R)-1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)-2-hydroxymethyl-4-(tert-butyldiphenylsilyloxy)piperidine(880548-65-2)
EPA Substance Registry System: (2S,4S,5R)-1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)-2-hydroxymethyl-4-(tert-butyldiphenylsilyloxy)piperidine(880548-65-2)

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: 880548-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 880548-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,0,5,4 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 880548-65:
(8*8)+(7*8)+(6*0)+(5*5)+(4*4)+(3*8)+(2*6)+(1*5)=202
202 % 10 = 2
So 880548-65-2 is a valid CAS Registry Number.

880548-65-2Upstream product

880548-65-2Downstream Products

880548-65-2Relevant academic research and scientific papers

A stereocontrolled formal asymmetric synthesis of pseudodistomin C

Tanaka, Ken-ichi,Maesoba, Takuya,Sawanishi, Hiroyuki

, p. 183 - 192 (2007/10/03)

An efficient and stereocontrolled formal asymmetric synthesis of pseudodistomin C has been achieved by employing intramolecular transamidation reaction, exo-methylenation, and highly stereoselective hydroboration. The resulting 2-hydroxymethylpiperidine d

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