Cas 289707-97-7,(S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-1-(2-benzyloxycarbonyl-ethylcarbamoyl)-2-tert-butoxycarbonylamino-butyl ester

289707-97-7

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Basic information

Product Name: (S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-1-(2-benzyloxycarbonyl-ethylcarbamoyl)-2-tert-butoxycarbonylamino-butyl ester
Synonyms: (S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-1-(2-benzyloxycarbonyl-ethylcarbamoyl)-2-tert-butoxycarbonylamino-butyl ester
CAS NO:289707-97-7
Molecular Formula:
Molecular Weight: 641.762
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: (S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-1-(2-benzyloxycarbonyl-ethylcarbamoyl)-2-tert-butoxycarbonylamino-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-1-(2-benzyloxycarbonyl-ethylcarbamoyl)-2-tert-butoxycarbonylamino-butyl ester(289707-97-7)
EPA Substance Registry System: (S)-2-Benzyloxycarbonylamino-4-methyl-pentanoic acid (S)-1-(2-benzyloxycarbonyl-ethylcarbamoyl)-2-tert-butoxycarbonylamino-butyl ester(289707-97-7)

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: 289707-97-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 289707-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,7,0 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 289707-97:
(8*2)+(7*8)+(6*9)+(5*7)+(4*0)+(3*7)+(2*9)+(1*7)=207
207 % 10 = 7
So 289707-97-7 is a valid CAS Registry Number.

289707-97-7Upstream product

289707-97-7Downstream Products

289708-18-5 3-[(S)-3-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-2-hydroxy-pentanoylamino]-propionic acid benzyl ester

289707-97-7Relevant academic research and scientific papers

Passerini multicomponent reaction of protected α-aminoaldehydes as a tool for combinatorial synthesis of enzyme inhibitors

Banfi, Luca,Guanti, Giuseppe,Riva, Renata

, p. 985 - 986 (2007/10/03)

Three-component Passerini condensation of N-Boc-α-aminoaldehydes with various isocyanides and carboxylic acids leads, after Boc- deprotection/transacylation, to complex peptide-like structures containing an α-hydroxy-β-aminoacid unit or, after oxidation,

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