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110811-31-9

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110811-31-9 Usage

General Description

4-Bromo-1-(tert-butoxycarbonyl)-1H-indole-3-carboxylic acid is a chemical compound with a molecular formula C16H16BrNO4. It is a derivative of indole, with a bromine atom and a tert-butoxycarbonyl group attached to the indole ring. 4-BROMO-1-(TERT-BUTOXYCARBONYL)-1H-INDOLE-3-CARBOXYLIC ACID has potential applications in pharmaceutical research and drug development, as indole derivatives are known for their diverse biological activities. The tert-butoxycarbonyl group is commonly used as a protective group in organic synthesis, and the bromine atom can serve as a versatile functional group for further chemical modifications. Further research is needed to explore the specific properties and potential uses of 4-bromo-1-(tert-butoxycarbonyl)-1H-indole-3-carboxylic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 110811-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,1 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110811-31:
(8*1)+(7*1)+(6*0)+(5*8)+(4*1)+(3*1)+(2*3)+(1*1)=69
69 % 10 = 9
So 110811-31-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrNO2/c10-6-2-1-3-7-8(6)5(4-11-7)9(12)13/h1-4,11H,(H,12,13)

110811-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-1H-indole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-bromo-3-indolecarboxylic acid

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:110811-31-9 SDS

110811-31-9Relevant articles and documents

Studies on the Claisen rearrangements in the indolo[2,3-b]quinoline system

Voute, Nicholas,Philp, Douglas,Slawin, Alexandra M. Z.,Westwood, Nicholas J.

supporting information; experimental part, p. 442 - 450 (2010/02/16)

A study of the effect of substrate structure on a Claisen-aza-Cope reaction is presented including a rationalisation of the reaction outcome using DFT calculations. An asymmetric version of the reaction is also described that is of relevance to a proposed

A CONVENIENT SYNTHETIC APPROACH TO 4-SUBSTITUTED INDOLES

Yamada, Fumio,Somei, Masanori

, p. 1173 - 1176 (2007/10/02)

A simple and practical synthetic method for 4-halogenoindoles, 4-indolecarbaldehyde, 4-cyanoindole, and 4-methoxycarbonylindole is elaborated.

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