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91828-08-9

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91828-08-9 Usage

General Description

3-Bromo-9-methyl-9H-carbazole is a chemical compound with the molecular formula C14H11BrN. It is a derivative of carbazole, a heterocyclic compound commonly found in coal tar and crude oil. This particular compound contains a bromine and a methyl group attached to the carbazole structure. It is used in the synthesis of organic compounds and as a reagent in various chemical reactions. The presence of the bromine and methyl groups make 3-Bromo-9-methyl-9H-carbazole a versatile building block for the preparation of a wide range of other organic compounds, including pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 91828-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91828-08:
(7*9)+(6*1)+(5*8)+(4*2)+(3*8)+(2*0)+(1*8)=149
149 % 10 = 9
So 91828-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H10BrN/c1-15-12-5-3-2-4-10(12)11-8-9(14)6-7-13(11)15/h2-8H,1H3

91828-08-9SDS

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 3-bromo-9-methylcarbazole

1.2 Other means of identification

Product number -
Other names 9H-Carbazole,3-bromo-9-methyl

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:91828-08-9 SDS

91828-08-9Relevant articles and documents

Redox-neutral decarboxylative photocyclization of anthranilic acids

Huang, Huawen,Deng, Kun,Deng, Guo-Jun

, p. 8243 - 8247 (2020/12/29)

A mild metal-, catalyst-, and oxidant-free photoredox neutral system has been found to efficiently enable intramolecular decarboxylative cyclization of anthranilic acids. This facile protocol provides an alternative method for the synthesis of carbazoles. Mechanistic studies reveal a key photoinduced 6π-electrocyclization process and formic acid was released as the sole byproduct.

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