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9H-Pyrido[3,4-b]indole, 3,6-dibromo-1-methyl- is a chemical compound with the molecular formula C10H8Br2N. It is a derivative of the pyridoindole class, characterized by the presence of a pyridine ring fused to an indole nucleus. This specific compound features two bromine atoms at the 3rd and 6th positions of the pyridoindole structure, and a methyl group at the 1st position. It is known for its potential applications in the synthesis of various biologically active compounds, such as alkaloids, due to its unique structure and reactivity. The compound is also of interest in the field of medicinal chemistry for its potential therapeutic properties.

144434-74-2

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144434-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144434-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,3 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144434-74:
(8*1)+(7*4)+(6*4)+(5*4)+(4*3)+(3*4)+(2*7)+(1*4)=122
122 % 10 = 2
So 144434-74-2 is a valid CAS Registry Number.

144434-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dibromo-1-methyl-9H-pyrido[3,4-b]indole

1.2 Other means of identification

Product number -
Other names OTJUQRPMEHCTRS-UHFFFAOYSA

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:144434-74-2 SDS

144434-74-2Upstream product

144434-74-2Downstream Products

144434-74-2Relevant academic research and scientific papers

A new method for bromination of carbazoles, β-carbolines and iminodibenzyls by use of N-bromosuccinimide and silica gel

Smith, Keith,Martin James,Mistry, Anil G.,Bye, Martin R.,John Faulkner

, p. 7479 - 7488 (2007/10/02)

Carbazole, N-ethylcarbazole, iminodibenzyl (10,11-dihydro-5H-dibenz[b,f]azepine), N-ethyliminodibenzyl and imipramine are readily mono-, di- or polybrominated in high yields at ambient temperature in dichloromethane by use of the appropriate quantity of N-bromosuccinimide in the presence of silica gel. By contrast, the brominations of the β-carbolines, harmane and norharman, are less selective and give mixtures of products, some of which have unusual substitution patterns.

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