Cas 71459-78-4,L-Methionine, N-[N-[N-[N-[N-[[(4-methoxyphenyl)methoxy]carbonyl]-L-tyrosyl]glycyl]glyc yl]-L-phenylalanyl]-, phenylmethyl ester

71459-78-4

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Basic information

Product Name: L-Methionine, N-[N-[N-[N-[N-[[(4-methoxyphenyl)methoxy]carbonyl]-L-tyrosyl]glycyl]glyc yl]-L-phenylalanyl]-, phenylmethyl ester
Synonyms:
CAS NO:71459-78-4
Molecular Formula: C43H49N5O10S
Molecular Weight: 827.956
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-Methionine, N-[N-[N-[N-[N-[[(4-methoxyphenyl)methoxy]carbonyl]-L-tyrosyl]glycyl]glyc yl]-L-phenylalanyl]-, phenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: L-Methionine, N-[N-[N-[N-[N-[[(4-methoxyphenyl)methoxy]carbonyl]-L-tyrosyl]glycyl]glyc yl]-L-phenylalanyl]-, phenylmethyl ester(71459-78-4)
EPA Substance Registry System: L-Methionine, N-[N-[N-[N-[N-[[(4-methoxyphenyl)methoxy]carbonyl]-L-tyrosyl]glycyl]glyc yl]-L-phenylalanyl]-, phenylmethyl ester(71459-78-4)

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: 71459-78-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71459-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,5 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71459-78:
(7*7)+(6*1)+(5*4)+(4*5)+(3*9)+(2*7)+(1*8)=144
144 % 10 = 4
So 71459-78-4 is a valid CAS Registry Number.

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71459-78-4Relevant academic research and scientific papers

A deblocking method using thioether-sulfonic acid systems. Application to the synthesis of met-enkephalin

Kiso,Ito,Nakamura,et al.

, p. 1472 - 1475 (1979)

Thioanisole-trifluoromethanesulfonic acid and thioanisole-methanesulfonic acid systems were found to be useful as deblocking methods in the synthesis of a methionine-containing peptide, Met-enkephalin, without any side reaction.

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