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163229-48-9

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163229-48-9 Usage

General Description

1-(tert-butyl) 2-methyl 1H-indole-1,2-dicarboxylate is a chemical compound with a molecular formula of C15H17NO4. It is a derivative of the indole-1,2-dicarboxylic acid, which is commonly used in the synthesis of pharmaceutical and organic compounds. This chemical is also known for its potential applications in the field of medicinal chemistry due to its biological activities. Its structure contains a tert-butyl group and a methyl group, and it is commonly used as a building block in the production of various drugs and related compounds. This chemical compound plays an important role in drug discovery and medicinal research due to its unique structure and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 163229-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,2,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 163229-48:
(8*1)+(7*6)+(6*3)+(5*2)+(4*2)+(3*9)+(2*4)+(1*8)=129
129 % 10 = 9
So 163229-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO4/c1-15(2,3)20-14(18)16-11-8-6-5-7-10(11)9-12(16)13(17)19-4/h5-9H,1-4H3

163229-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-tert-butyl 2-O-methyl indole-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1-tert-butyl 2-methyl 1H-indole-1,2-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:163229-48-9 SDS

163229-48-9Relevant articles and documents

Enantioselective Borylative Dearomatization of Indoles through Copper(I) Catalysis

Kubota, Koji,Hayama, Keiichi,Iwamoto, Hiroaki,Ito, Hajime

, p. 8809 - 8813 (2015)

The enantioselective borylative dearomatization of a heteroaromatic compound has been achieved using a copper(I) catalyst and a diboron reagent. This reaction involves the regio- and enantioselective addition of active borylcopper(I) species to indole-2-carboxylates, followed by the diastereoselective protonation of the resulting copper(I) enolate to give the corresponding chiral indolines, which bear consecutive stereogenic centers.

Redox-Neutral Photocatalytic C?H Carboxylation of Arenes and Styrenes with CO2

Bergonzini, Giulia,Brandt, Peter,Fricke, Florian,Johansson, Magnus J.,K?nig, Burkhard,Schmalzbauer, Matthias,Svejstrup, Thomas D.

supporting information, p. 2658 - 2672 (2020/10/07)

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CAFFEINE INHIBITORS OF MTHFD2 AND USES THEREOF

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Paragraph 000753; 000754, (2017/07/06)

The present invention provides compounds, compositions thereof, and methods of using the same.

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