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Phenol, 2-chloro-4-[(4-chlorophenyl)azo]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16434-26-7

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16434-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16434-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,3 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16434-26:
(7*1)+(6*6)+(5*4)+(4*3)+(3*4)+(2*2)+(1*6)=97
97 % 10 = 7
So 16434-26-7 is a valid CAS Registry Number.

16434-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-[(4-chlorophenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-chloro-4-(4-chloro-phenylazo)-phenol

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:16434-26-7 SDS

16434-26-7Relevant academic research and scientific papers

Synthesis and characterization of azo compounds and study of the effect of substituents on their liquid crystalline behavior

Al-Hamdani, Uhood J.,Gassim, Tarik E.,Radhy, Howraa H.

experimental part, p. 5620 - 5628 (2010/12/18)

In this paper we present six select mesomorphic azo compounds distinguished by the presence of diverse substituents on a central benzene nucleus. All the synthesized compounds exhibit enantiotropic mesophases. The mesomorphic properties of the substituted compounds were compared with those of the unsubstituted parent compound to evaluate the effect of the nature and position of the substituents on mesomorphism.

Reaction of Haloazoxybenzenes with Sulfuric Acid

Shimao, Ichiro,Fujimori, Ken,Oae, Shigeru

, p. 546 - 550 (2007/10/02)

Treatment of 4,4'-dihaloazoxybenzenes with sulfuric acid afforded 4,4'-dihaloazobenzenes (6) as the major product and 5-halo-2-(p-halophenylazo)phenols, the Wallach rearrangement products as minor products, besides 2-halo-5-(halophenylazo)phenols, 2-halo-4-(p-halophenylazo)phenols, and 4-(p-halophenylazo)phenols as abnormal rearrangement products.The reaction of fluoro compounds gave the azophenols (3a or 5a) in the best yields.However, the ratio of 3a to 5a was found to vary with the concentration of sulfuric acid.Treatment of 4-haloazoxybenzenes with sulfuric acid gave 4-(p-halophenylazo)phenols and 4-haloazobenzenes (13) as major products together with 2-(p-halophenylazo)phenols and 5-halo-2-(phenylazo)phenols as minor products.Yields of reduction products 6 and 13 increased as the halosubstituent became heavier in the following sequence: F -> Cl -> Br -> I.

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