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D-Tryptophan, 1-methyl-N-[(4-nitrophenyl)sulfonyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

919787-35-2

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919787-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 919787-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,7,8 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 919787-35:
(8*9)+(7*1)+(6*9)+(5*7)+(4*8)+(3*7)+(2*3)+(1*5)=232
232 % 10 = 2
So 919787-35-2 is a valid CAS Registry Number.

919787-35-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-methyl-1H-indol-3-yl)-2-(4-nitro-benzenesulfonylamino)-propionic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:919787-35-2 SDS

919787-35-2Downstream Products

919787-35-2Relevant academic research and scientific papers

Synthesis of chiral 3-substituted hexahydropyrroloindoline via intermolecular cyclopropanation

Song, Hao,Yang, Jun,Chen, Wei,Qin, Yong

, p. 6011 - 6014 (2007/10/03)

(Chemical Equation Presented) A new and efficient synthetic route to chiral 3-substituted hexahydropyrroloindoline 18 possessing absolute configurations in accordance with indole alkaloids has been developed from readily available L-tryptophan. The key step relies on the one-pot cascade reaction of oxazolidinone 17 with diazoester, which proceeds through intermolecular cyclopropanation, ring opening, and cyclization.

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