Cas 269733-29-1,(S)-6-tert-Butoxycarbonylamino-2-(triphenylphosphoranylidene)-3-oxoheptanedioic acid di-tert-butyl ester

269733-29-1

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Basic information

Product Name: (S)-6-tert-Butoxycarbonylamino-2-(triphenylphosphoranylidene)-3-oxoheptanedioic acid di-tert-butyl ester
Synonyms: (S)-6-tert-Butoxycarbonylamino-2-(triphenylphosphoranylidene)-3-oxoheptanedioic acid di-tert-butyl ester
CAS NO:269733-29-1
Molecular Formula:
Molecular Weight: 661.775
EINECS: N/A
Product Categories: N/A
Mol File: 269733-29-1.mol
Article Data: 2

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: (S)-6-tert-Butoxycarbonylamino-2-(triphenylphosphoranylidene)-3-oxoheptanedioic acid di-tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-6-tert-Butoxycarbonylamino-2-(triphenylphosphoranylidene)-3-oxoheptanedioic acid di-tert-butyl ester(269733-29-1)
EPA Substance Registry System: (S)-6-tert-Butoxycarbonylamino-2-(triphenylphosphoranylidene)-3-oxoheptanedioic acid di-tert-butyl ester(269733-29-1)

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: 269733-29-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 269733-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,7,3 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 269733-29:
(8*2)+(7*6)+(6*9)+(5*7)+(4*3)+(3*3)+(2*2)+(1*9)=181
181 % 10 = 1
So 269733-29-1 is a valid CAS Registry Number.

269733-29-1Upstream product

269733-29-1Downstream Products

269733-29-1Relevant articles and documents

A versatile synthetic route to quinoxaline, pyrazine and 1,2,4-triazine substituted α-amino acids from vicinal tricarbonyls

Adlington, Robert M.,Baldwin, Jack E.,Catterick, David,Pritchard, Gareth J.

, p. 299 - 302 (2000)

A range of novel heterocyclic α-amino acids has been synthesised by the reaction of diamines and amidrazones with α-amino acid vicinal tricarbonyl reactive substrates. The Royal Society of Chemistry 2000.

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