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164736-47-4

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164736-47-4 Usage

General Description

7-Bromo-1,2,3,4-tetrahydrocyclopenta[b]indole is a chemical compound with a molecular formula of C11H11BrN. It is a brominated derivative of tetrahydrocyclopenta[b]indole and has a fused pentacyclic structure, making it a heterocyclic compound. This chemical is commonly used as a starting material in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential pharmacological activities, particularly as a serotonin receptor agonist, which makes it a valuable compound in the field of medicinal chemistry and drug discovery. Additionally, its unique structure and properties make it a valuable tool for researchers and chemists in diverse fields.

Check Digit Verification of cas no

The CAS Registry Mumber 164736-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,7,3 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 164736-47:
(8*1)+(7*6)+(6*4)+(5*7)+(4*3)+(3*6)+(2*4)+(1*7)=154
154 % 10 = 4
So 164736-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClNO/c8-6-3-5(4-9)1-2-7(6)10/h1-3,10H

164736-47-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H50592)  7-Bromo-1,2,3,4-tetrahydrocyclopent[b]indole, 99%   

  • 164736-47-4

  • 250mg

  • 607.0CNY

  • Detail
  • Alfa Aesar

  • (H50592)  7-Bromo-1,2,3,4-tetrahydrocyclopent[b]indole, 99%   

  • 164736-47-4

  • 1g

  • 2423.0CNY

  • Detail

164736-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Bromo-1,2,3,4-tetrahydrocyclopenta[b]indole

1.2 Other means of identification

Product number -
Other names 7-BROMO-1,2,3,4-TETRAHYDROCYCLOPENTA[B]INDOLE

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:164736-47-4 SDS

164736-47-4Downstream Products

164736-47-4Relevant articles and documents

Heterocyclic com pounds and organic light-emitting diode including the same

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Paragraph 0279; 0292-0297, (2019/08/30)

PURPOSE: A heterocyclic compound and an organic electroluminescent device containing the same are provided to show stability compared with an existing material and to have superior light emitting properties such as low driving voltage or current efficiency. CONSTITUTION: A heterocyclic compound is denoted by chemical formula 1. An organic electroluminescent device comprises an anode, a cathode, and layers containing the heterocyclic compounds, which is placed between the anode and the cathode. A light emitting layer between the anode and the cathode contains the heterocyclic compounds. The organic electroluminescent device further comprises one or more layers selected among a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, and an electron injection layer.

Aromatic compound and organoelectroluminescent device comprising the compound

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Paragraph 0257-0263, (2019/12/10)

The present invention relates to a novel aromatic compound and an organic electroluminescent device comprising the same. The present invention relates to an organic electroluminescent device including an aromatic compound. (by machine translation)

A facile approach to the synthesis of 5,7-disubstituted indoles via a highly selective lithium-bromine exchange of 5,7-dibromoindoles

Li, Lianhai,Martins, Andrew

, p. 689 - 692 (2007/10/03)

A general approach to the synthesis of 5,7-disubstituted indoles has been developed based upon a highly selective lithium-bromine exchange reaction at the 7-position when 1-alkyl-5,7-dibromoindoles were treated with t-BuLi in ether. The resulting 5-bromo-7-lithiated indoles could react with various electrophiles to afford 5-bromo-7-substituted indoles (6) upon work-up. Without isolation of 6, the intermediates thus obtained could be exposed to a second lithium-bromine exchange reaction in a one-pot procedure and further reacted with various electrophiles to afford 5,7-disubstituted indoles (1).

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