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Ethanone, 1-(4-butoxy-2-hydroxyphenyl)-, [1-(4-butoxy-2-hydroxyphenyl)ethylidene]hydrazone is a complex organic compound with the chemical formula C16H22O3. It is a derivative of acetone, featuring a 4-butoxy-2-hydroxyphenyl group attached to the acetone molecule. Ethanone, 1-(4-butoxy-2-hydroxyphenyl)-, [1-(4-butoxy-2-hydroxyphenyl)ethylidene]hydrazone is characterized by the presence of a hydrazone functional group, which is formed by the reaction of the acetone's carbonyl group with a hydrazine derivative. The compound has a molecular weight of 262.34 g/mol and is likely to be a solid at room temperature. It is an example of a substituted acetophenone, with the butoxy and hydroxy substituents on the phenyl ring influencing its chemical properties and potential applications, which may include use in the synthesis of pharmaceuticals or other organic compounds.

2680-49-1

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2680-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2680-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2680-49:
(6*2)+(5*6)+(4*8)+(3*0)+(2*4)+(1*9)=91
91 % 10 = 1
So 2680-49-1 is a valid CAS Registry Number.

2680-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-dibutoxy-2,2'-dihydroxy-α,α'-dimethylbenzalazine

1.2 Other means of identification

Product number -
Other names -

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:2680-49-1 SDS

2680-49-1Downstream Products

2680-49-1Relevant academic research and scientific papers

SYNTHESIS AND MESOMORPHIC PROPERTIES OF THREE HOMOLOGOUS SERIES OF 4,4 prime -DIALKOXY- alpha , alpha prime -DIMETHYLBENZALAZINES.

Marcos,Melendez,Serrano

, p. 157 - 172 (2007/10/02)

Three homologous series of alpha , alpha prime -dimethylbenzalazines have been synthesized: 4,4 prime -dialkoxy- alpha , alpha prime -dimethylbenzalazines, 4,4 prime -dialkoxy-2,2 prime -dihydroxy- alpha , alpha prime -dimethylbenzalazines, and 4,4 prime -dialkoxy-2-hydroxy- alpha , alpha prime -dimethylbenzalazines. The influence of molecular structure on the mesomorphic properties was studied. Mesomorphic properties and phase transitions were determined using a polarizing hot-stage microscope and a differential scanning calorimeter. The introduction of one or two hydroxyl groups in position 2- or 2-and 2 prime -of the aromatic rings (4,4 prime -dialkoxy-2-hydroxy- alpha , alpha prime -dimethylbenzalazines and 4,4 prime -dialkoxy-2,2 prime -dihydroxy- alpha , alpha prime -dimethylbenzalazines respectively) gives molecules with an excellent mesogenic quality, and all the prepared compounds of these series exhibit mesomorphism. Compounds of the series with two hydroxyl groups exhibit smectic polymorphism which is not so in the case of the compounds of the other series. The melting temperatures are systematically lower for the 4,4 prime -dialkoxy-2-hydroxy- alpha , alpha prime -dimethylbenzalazines than for the other two series.

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