Cas 96238-72-1,L-Leucine, N-[1-[(1,1-dimethylethoxy)carbonyl]-N-[N-[(1,1-dimethylethoxy)carbonyl] -L-phenylalanyl]-L-tryptophyl]-, methyl ester

96238-72-1

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Basic information

Product Name: L-Leucine, N-[1-[(1,1-dimethylethoxy)carbonyl]-N-[N-[(1,1-dimethylethoxy)carbonyl] -L-phenylalanyl]-L-tryptophyl]-, methyl ester
Synonyms:
CAS NO:96238-72-1
Molecular Formula: C37H50N4O8
Molecular Weight: 678.826
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: L-Leucine, N-[1-[(1,1-dimethylethoxy)carbonyl]-N-[N-[(1,1-dimethylethoxy)carbonyl] -L-phenylalanyl]-L-tryptophyl]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: L-Leucine, N-[1-[(1,1-dimethylethoxy)carbonyl]-N-[N-[(1,1-dimethylethoxy)carbonyl] -L-phenylalanyl]-L-tryptophyl]-, methyl ester(96238-72-1)
EPA Substance Registry System: L-Leucine, N-[1-[(1,1-dimethylethoxy)carbonyl]-N-[N-[(1,1-dimethylethoxy)carbonyl] -L-phenylalanyl]-L-tryptophyl]-, methyl ester(96238-72-1)

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: 96238-72-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96238-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,3 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96238-72:
(7*9)+(6*6)+(5*2)+(4*3)+(3*8)+(2*7)+(1*2)=161
161 % 10 = 1
So 96238-72-1 is a valid CAS Registry Number.

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96238-72-1Relevant academic research and scientific papers

Synthesis, Properties, and Use of Nin-Boc-tryptophan Derivatives

Franzen, Henry,Grehn, Leif,Ragnarsson, Ulf

, p. 1699 - 1700 (1984)

Nin-Boc-protected tryptophan derivatives can be prepared with Boc2O-4-dimethylaminopyridine in MeCN; their properties and utility are demonstrated in the synthesis of a tryptophan-containing tetrapeptide related to substance P.

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