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2,5-Cyclohexadiene-1,4-dione, 5-bromo-2,3-dimethyl-, also known as 5-bromo-2,3-dimethylcyclohexa-2,5-diene-1,4-dione, is a brominated derivative of the cyclic diketone 2,5-Cyclohexadiene-1,4-dione. It has the molecular formula C8H9BrO2 and is a yellow solid at room temperature. This chemical compound is known for its unique structure and properties, making it a promising candidate for various applications in organic synthesis and pharmaceutical production.

13070-27-4

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13070-27-4 Usage

Uses

Used in Organic Synthesis:
2,5-Cyclohexadiene-1,4-dione, 5-bromo-2,3-dimethylis used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Production:
2,5-Cyclohexadiene-1,4-dione, 5-bromo-2,3-dimethylis utilized in the production of pharmaceuticals due to its potential to be incorporated into the molecular structures of new drugs, enhancing their therapeutic properties and effectiveness.
Used in Drug Development:
2,5-Cyclohexadiene-1,4-dione, 5-bromo-2,3-dimethylhas potential uses in the development of new drugs, as its unique structure and properties can be leveraged to create novel therapeutic agents with improved pharmacological profiles.
Used in Material Science:
Due to its unique chemical and physical properties, 2,5-Cyclohexadiene-1,4-dione, 5-bromo-2,3-dimethylmay also find applications in the development of new materials with specific characteristics, such as improved stability or reactivity, for use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13070-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,7 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13070-27:
(7*1)+(6*3)+(5*0)+(4*7)+(3*0)+(2*2)+(1*7)=64
64 % 10 = 4
So 13070-27-4 is a valid CAS Registry Number.

13070-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-2,3-dimethylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 6-bromo-2,3-dimethyl-p-benzoquinone

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:13070-27-4 SDS

13070-27-4Relevant academic research and scientific papers

Convergent synthesis of 2H-chromenes - A formal [3+3] cycloaddition by a one-pot, three-step cascade

Parker, Kathlyn A.,Mindt, Thomas L.

experimental part, p. 9779 - 9786 (2012/02/05)

In cases in which the palladium-catalyzed coupling of a bromoquinone with a vinyl stannane affords a vinyl quinone that enolizes, the resulting ortho-quinone methide undergoes an oxa-6π electrocyclization. Enolization is promoted by the presence of a pola

Synthesis and spectroscopic characterization of 1-13C- and 4-13C-plastoquinone-9

Boers, Rutger B.,Randulfe, Yolanda Pazos,Van Der Haas, Hendrikus N. S.,Van Rossum-Baan, Marleen,Lugtenburg, Johan

, p. 2094 - 2108 (2007/10/03)

This paper presents the synthesis of 1-13C- and 4-13C-plastoquinone-9 and their characterization with NMR spectroscopy and mass spectrometry. The synthetic scheme has been further adapted to introduce 13C-labeled plastoquinones on all individual and on each combination of positions in the quinone ring. Also a two-step scheme is disclosed to prepare unlabeled plastoquinone-9. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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