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957127-83-2

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957127-83-2 Usage

General Description

N-BOC-1H-indole-6-carboxylic acid methyl ester is a chemical compound commonly used in organic synthesis and medicinal chemistry. It is a derivative of indole, a heterocyclic aromatic compound, and is often used as a building block for the synthesis of biologically active molecules. The "N-BOC" group refers to the tert-butyloxycarbonyl protecting group, which is commonly used in organic synthesis to protect functional groups. The methyl ester functional group makes this compound useful for further chemical modifications, and its indole core structure provides potential pharmacological activity. Overall, N-BOC-1H-indole-6-carboxylic acid methyl ester is a versatile and valuable compound in chemical research and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 957127-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,1,2 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 957127-83:
(8*9)+(7*5)+(6*7)+(5*1)+(4*2)+(3*7)+(2*8)+(1*3)=202
202 % 10 = 2
So 957127-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO4/c1-15(2,3)20-14(18)16-8-7-10-5-6-11(9-12(10)16)13(17)19-4/h5-9H,1-4H3

957127-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-tert-butyl 6-O-methyl indole-1,6-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1-tert-Butyl 6-methyl 1H-indole-1,6-dicarboxylate

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:957127-83-2 SDS

957127-83-2Downstream Products

957127-83-2Relevant articles and documents

Intermodular decarboxylative direct C-3 arylation of indoles with benzoic acids

Cornelia, Josep,Lu, Pengfel,Larrosa, Igor

supporting information; experimental part, p. 5506 - 5509 (2010/02/28)

"Chemical Equation Presented" A palladium catalyzed C-H activation of indoles and a silver catalyzed decarboxylative C-C activation of ortho substituted benzoic acids are synergistically combined to synthesize indoles arylated exclusively In the C-3 posit

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