Cas 133641-14-2,N-(tert-butyloxycarbonyl)-3-(3-formyl-4-methoxyphenyl)-L-alanine

133641-14-2

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Basic information

Product Name: N-(tert-butyloxycarbonyl)-3-(3-formyl-4-methoxyphenyl)-L-alanine
Synonyms: N-(tert-butyloxycarbonyl)-3-(3-formyl-4-methoxyphenyl)-L-alanine
CAS NO:133641-14-2
Molecular Formula:
Molecular Weight: 323.346
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: N-(tert-butyloxycarbonyl)-3-(3-formyl-4-methoxyphenyl)-L-alanine(CAS DataBase Reference)
NIST Chemistry Reference: N-(tert-butyloxycarbonyl)-3-(3-formyl-4-methoxyphenyl)-L-alanine(133641-14-2)
EPA Substance Registry System: N-(tert-butyloxycarbonyl)-3-(3-formyl-4-methoxyphenyl)-L-alanine(133641-14-2)

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: 133641-14-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133641-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 133641-14:
(8*1)+(7*3)+(6*3)+(5*6)+(4*4)+(3*1)+(2*1)+(1*4)=102
102 % 10 = 2
So 133641-14-2 is a valid CAS Registry Number.

133641-14-2Upstream product

574735-09-4 2-tert-butoxycarbonylamino-3-(3-formyl-4-methoxy-phenyl)-propionic acid methyl ester

133641-14-2Downstream Products

35296-56-1 3-(3-hydroxy-4-methoxyphenyl)-L-alanine

133641-14-2Relevant academic research and scientific papers

Synthesis of tyrosine derivatives for saframycin MX1 biosynthetic studies

Schmidt, Eric W.,Nelson, James T.,Fillmore, John P.

, p. 3921 - 3924 (2007/10/03)

Saframycin MX1 and structural relatives are natural anticancer agents isolated from bacteria and marine invertebrates. For biosynthetic studies and to make a library of modified natural products, a series of tyrosine derivatives were synthesized in a conc

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