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3-bromo-2-methyl-5-(propan-2-yl)cyclohexa-2,5-diene-1,4-dione is a complex organic compound with the molecular formula C11H15BrO2. It features a cyclohexa-2,5-diene-1,4-dione core, which is a six-membered ring with two carbonyl groups (C=O) at positions 1 and 4. The molecule also contains a bromine atom at the 3-position, a methyl group (CH3) at the 2-position, and a propan-2-yl group (C3H7) at the 5-position. 3-bromo-2-methyl-5-(propan-2-yl)cyclohexa-2,5-diene-1,4-dione is characterized by its unique structure and functional groups, which may contribute to its potential applications in various chemical and industrial processes.

6307-97-7

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6307-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6307-97-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6307-97:
(6*6)+(5*3)+(4*0)+(3*7)+(2*9)+(1*7)=97
97 % 10 = 7
So 6307-97-7 is a valid CAS Registry Number.

6307-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2-methyl-5-propan-2-ylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 3-bromo-5-isopropyl-2-methylcyclohexa-2,5-diene-1,4-dione

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:6307-97-7 SDS

6307-97-7Relevant academic research and scientific papers

Regioselective alkylation of heteroaromatic compounds with 3-methyl-2-quinonyl boronic acids

Veguillas, Marcos,Ribagorda, Maria,Carreno, M. Carmen

supporting information; experimental part, p. 656 - 659 (2011/04/24)

Reactions of heteroaromatic compounds with 3-methyl substituted 2-quinonyl boronic acids proceeded by 1,4-addition followed by spontaneous protodeboronation, leading directly to the Friedel-Crafts alkylation products instead of the commonly observed alken

Facile Oxidation of Halophenols and Halonaphthols by Ceric Ammonium Sulphate and Manganic Sulphate

Gopinathan, M. B.,Bhatt, M. Vivekananda

, p. 71 - 72 (2007/10/02)

Ce(IV) and Mn(III) sulphates oxidise halophenols and halonaphthols in aqueous acetonitrile medium to the corresponding haloquinones in high yields.

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