Cas 610772-74-2,(2R,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one

610772-74-2

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Basic information

Product Name: (2R,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one
Synonyms: (2R,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one
CAS NO:610772-74-2
Molecular Formula:
Molecular Weight: 581.712
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,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one(610772-74-2)
EPA Substance Registry System: (2R,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one(610772-74-2)

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: 610772-74-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 610772-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,7,7 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 610772-74:
(8*6)+(7*1)+(6*0)+(5*7)+(4*7)+(3*2)+(2*7)+(1*4)=142
142 % 10 = 2
So 610772-74-2 is a valid CAS Registry Number.

610772-74-2Upstream product

610772-74-2Downstream Products

610772-74-2Relevant academic research and scientific papers

Synthesis of 2,6-disubstituted piperidine-bearing α-amino acid side-chains

Boeglin, Damien,Heitz, Annie,Martinez, Jean,Fehrentz, Jean-Alain

, p. 3139 - 3146 (2007/10/03)

A straightforward synthesis of 2,6-disubstituted piperidines bearing α-amino acid side-chains was developed. Synthesis was based on a Horner-Wadsworth-Emmons condensation of a β-ketophosphonate derived from an α-amino acid residue with a β-homologated ald

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