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86309-06-0

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86309-06-0 Usage

General Description

2-(2,4-Dichlorophenoxy)benzenecarbaldehyde is a chemical compound with the molecular formula C13H8Cl2O2. It is a white to off-white crystalline solid that is insoluble in water but soluble in organic solvents. 2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE is commonly used in the synthesis of pharmaceuticals and agrochemicals. It is also used as an intermediate in the production of dyes, pigments, and other organic compounds. Additionally, it has been studied as a potential herbicide for weed control. However, it is important to handle this chemical with caution, as it may be harmful if swallowed, inhaled, or comes into contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 86309-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,0 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86309-06:
(7*8)+(6*6)+(5*3)+(4*0)+(3*9)+(2*0)+(1*6)=140
140 % 10 = 0
So 86309-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H8Cl2O2/c14-10-5-6-13(11(15)7-10)17-12-4-2-1-3-9(12)8-16/h1-8H

86309-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dichlorophenoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names dichlorophenoxybenzenecarbaldehyde

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:86309-06-0 SDS

86309-06-0Relevant articles and documents

Discovery of Pyrazine-Carboxamide-Diphenyl-Ethers as Novel Succinate Dehydrogenase Inhibitors via Fragment Recombination

Li, Hua,Gao, Meng-Qi,Chen, Yan,Wang, Yu-Xia,Zhu, Xiao-Lei,Yang, Guang-Fu

, p. 14001 - 14008 (2020/11/27)

The discovery of novel succinate dehydrogenase inhibitors (SDHIs) has attracted great attention worldwide. Herein, a fragment recombination strategy was proposed to design new SDHIs by understanding the ligand-receptor interaction mechanism of SDHIs. Thre

Rearrangement of 2-aryloxybenzaldehydes to 2-hydroxybenzophenones by rhodium-catalyzed cleavage of aryloxy C-O bonds

Rao, Honghua,Li, Chao-Jun

supporting information; experimental part, p. 8936 - 8939 (2011/11/07)

Lost in the shuffle: An unprecedented rearrangement of the title compounds proceeds by the simultaneous rhodium-catalyzed cleavage of aryloxy C-O and aldehyde C-H bonds (see scheme). The reaction tolerates the presence of various catalytically reactive substituents such as aryl halides, nitrile, and esters.

Imidazo heterocyclic compounds

-

, (2011/07/06)

A novel class of imidazo heterocyclic compounds, pharmaceutical compositions comprising them and use thereof in the treatment and/or prevention of diseases and disorders related to the histamine H3 receptor. More particularly, the compounds are useful for the treatment and/or prevention of diseases and disorders in which an interaction with the histamine H3 receptor is beneficial.

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