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126517-23-5

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126517-23-5 Usage

Properties

1. Chemical formula: C13H10Cl2O
2. Contains a 3-chlorophenyl group
3. Used in chemical reactions and organic synthesis
4. Potential applications in pharmaceutical and agricultural industries
5. Handle with caution due to hazardous properties

Specific Content

Chlorinated derivative of benzenemethanol
Contains a 3-chlorophenyl group
Used in chemical reactions and organic synthesis processes
Potential applications in pharmaceutical and agricultural industries
Should be handled with caution and accordance with proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 126517-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,1 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126517-23:
(8*1)+(7*2)+(6*6)+(5*5)+(4*1)+(3*7)+(2*2)+(1*3)=115
115 % 10 = 5
So 126517-23-5 is a valid CAS Registry Number.

126517-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3'-dichloro-benzhydrol

1.2 Other means of identification

Product number -
Other names 2,3'-Dichlor-benzhydrol

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:126517-23-5 SDS

126517-23-5Relevant articles and documents

POTENTIAL ANTICONVULSANTS: 3-CHLOROBENZOPHENONE DERIVATIVES

Jilek, Jiri,Urban, Jiri,Kmonicek, Vojtech,Pomykacek, Josef,Holubek, Jiri,et al.

, p. 2248 - 2260 (2007/10/02)

Reactions of 2-(2-iodoacetamido)-5-chlorobenzophenone with 2-amino-2-phenylethanol, 2-amino-1-phenylethanol, 3-amino-2-phenylpropanol, D(+)-norpseudoephedrine, and 2-aminopropane-2-carbonitrile gave the 2-substituted N-(2-benzoyl-4-chlorophenyl)acetamides X-XIV. 2,3'-Dichlorobenzhydrol (XVI) and 2,3'-dichlorobenzhydryl chloride (XIX) were transformed to the ethers XVII and XVIII and to the amines XXI-XXIV.Compound XVI was oxidized to the ketone XXV which was transformed via the oxime XXVI to compound XXVII.The basic products were converted to salts which were pharmacologically tested.Compounds X, XVII, XXIII, and XXVII showed anticonvulsant effects and some other neurotropic activities.

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