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24988-36-1

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24988-36-1 Usage

General Description

1,5-Dibromo-2,4-dimethoxybenzene is a chemical compound with the molecular formula C8H8Br2O2. It is a yellow solid at room temperature and is insoluble in water. 1,5-Dibromo-2,4-dimethoxybenzene is commonly used as an intermediate in the synthesis of various organic compounds, such as pharmaceuticals and agrochemicals. It is also used as a reagent in organic chemistry reactions, particularly in the preparation of biaryl compounds and other aromatic compounds. 1,5-Dibromo-2,4-dimethoxybenzene is considered to be a hazardous substance and should be handled with care due to its potential harmful effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 24988-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,8 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24988-36:
(7*2)+(6*4)+(5*9)+(4*8)+(3*8)+(2*3)+(1*6)=151
151 % 10 = 1
So 24988-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Br2O2/c1-11-7-4-8(12-2)6(10)3-5(7)9/h3-4H,1-2H3

24988-36-1SDS

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 1,5-Dibromo-2,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 1,3-dibromo-4,6-dimethoxybenzene

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:24988-36-1 SDS

24988-36-1Relevant articles and documents

Micelle-like molecular capsules with anthracene shells as photoactive hosts

Kondo, Kei,Suzuki, Akira,Akita, Munetaka,Yoshizawa, Michito

, p. 2308 - 2312 (2013)

Aromatic micelles: Hydrophobic and aromatic-aromatic interactions promoted the spontaneous formation of micelle-inspired molecular capsules with large aromatic shells from bent bisanthracene amphiphiles (see picture). The micellar capsules could accommoda

Compound

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Paragraph 0257-0259, (2020/05/02)

PROBLEM TO BE SOLVED: To provide a compound capable of forming a color filter excellent in heat resistance. SOLUTION: The present invention provides a compound represented by formula (I). [In formula (I), R1-R8 independently represen

Organic semiconductor photocatalyst can bifunctionalize arenes and heteroarenes

Ghosh, Indrajit,Khamrai, Jagadish,Savateev, Aleksandr,Shlapakov, Nikita,Antonietti, Markus,K?nig, Burkhard

, p. 360 - 366 (2019/08/15)

Photoexcited electron-hole pairs on a semiconductor surface can engage in redox reactions with two different substrates. Similar to conventional electrosynthesis, the primary redox intermediates afford only separate oxidized and reduced products or, more rarely, combine to one addition product. Here, we report that a stable organic semiconductor material, mesoporous graphitic carbon nitride (mpg-CN), can act as a visible-light photoredox catalyst to orchestrate oxidative and reductive interfacial electron transfers to two different substrates in a two- or three-component system for direct twofold carbon–hydrogen functionalization of arenes and heteroarenes. The mpg-CN catalyst tolerates reactive radicals and strong nucleophiles, is straightforwardly recoverable by simple centrifugation of reaction mixtures, and is reusable for at least four catalytic transformations with conserved activity.

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