Cas 86658-81-3,3-(5-Bromo-1H-indol-3-yl)-2-(toluene-4-sulfonylamino)-propionic acid methyl ester

86658-81-3

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Basic information

Product Name: 3-(5-Bromo-1H-indol-3-yl)-2-(toluene-4-sulfonylamino)-propionic acid methyl ester
Synonyms:
CAS NO:86658-81-3
Molecular Formula:
Molecular Weight: 451.341
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: 3-(5-Bromo-1H-indol-3-yl)-2-(toluene-4-sulfonylamino)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(5-Bromo-1H-indol-3-yl)-2-(toluene-4-sulfonylamino)-propionic acid methyl ester(86658-81-3)
EPA Substance Registry System: 3-(5-Bromo-1H-indol-3-yl)-2-(toluene-4-sulfonylamino)-propionic acid methyl ester(86658-81-3)

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: 86658-81-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86658-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,5 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86658-81:
(7*8)+(6*6)+(5*6)+(4*5)+(3*8)+(2*8)+(1*1)=183
183 % 10 = 3
So 86658-81-3 is a valid CAS Registry Number.

86658-81-3Upstream product

67488-65-7 (RS)-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid methyl ester

86658-81-3Downstream Products

86658-81-3Relevant academic research and scientific papers

A GENERAL METHOD FOR THE SYNTHESIS OF INDOLES BEARING A VARIETY OF SUBSTITUENTS AT THE β-POSITION, AND ITS APPLICATION TO THE SYNTHESIS OF L-TRYPTOPHAN

Shono, Tatsuya,Matsumura, Yoshihiro,Kanazawa, Takenobu

, p. 1259 - 1262 (2007/10/02)

A general synthetic method of β-substituted indoles such as indolacetic acid, tryptamine and L-tryptophan has been exploited utilizing α-methoxylated amides, lactams, a carbamate, and sulfonamides, easily obtainable by an electrochemical method, as key intemediates.

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