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1202362-88-6

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1202362-88-6 Usage

General Description

3-Methyl-9-phenyl-9H-carbazole is a chemical compound belonging to the class of organic molecules known as carbazoles. These are aromatic heterocyclic compounds containing a three-ring system with two benzene rings fused onto a five-membered nitrogen-containing ring. Specifically, in 3-Methyl-9-phenyl-9H-carbazole, the benzene ring is linked to the five-membered ring at the 9th position and a methyl group at the 3rd position. This aromatic compound is frequently used in the field of organic synthesis and in the creation of certain types of dyes. Its properties and structure enable its prevalent use in chemical research and in the development of new materials.

Check Digit Verification of cas no

The CAS Registry Mumber 1202362-88-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,3,6 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1202362-88:
(9*1)+(8*2)+(7*0)+(6*2)+(5*3)+(4*6)+(3*2)+(2*8)+(1*8)=106
106 % 10 = 6
So 1202362-88-6 is a valid CAS Registry Number.

1202362-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-9-phenylcarbazole

1.2 Other means of identification

Product number -
Other names 3-Methyl-9-phenyl-9h-carbazole

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:1202362-88-6 SDS

1202362-88-6Relevant 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.

Palladium-Catalyzed Methylation of Aryl, Heteroaryl, and Vinyl Boronate Esters

Haydl, Alexander M.,Hartwig, John F.

supporting information, p. 1337 - 1341 (2019/02/26)

A method for the direct methylation of aryl, heteroaryl, and vinyl boronate esters is reported, involving the reaction of iodomethane with aryl-, heteroaryl-, and vinylboronate esters catalyzed by palladium and PtBu2Me. This transformation occurs with a remarkably broad scope and is suitable for late-stage derivatization of biologically active compounds via the boronate esters. The unique capabilities of this method are demonstrated by combining carbon-boron bond-forming reactions with palladium-catalyzed methylation in a tandem transformation.

Photochemical Synthesis of Carbazoles Using an [Fe(phen)3](NTf2)2/O2 Catalyst System: Catalysis toward Sustainability

Parisien-Collette, Shawn,Hernandez-Perez, Augusto C.,Collins, Shawn K.

supporting information, p. 4994 - 4997 (2016/10/14)

An increasingly sustainable photochemical synthesis of carbazoles was developed using a catalytic system of Fe(phen)3(NTf2)2/O2 under continuous flow conditions and was demonstrated on gram-scale using a numbering-up strategy. Photocyclization of triaryl and diarylamines into the corresponding carbazoles occurs in general in higher yields than with previously developed photocatalysts.

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