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1726-78-9

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1726-78-9 Usage

General Description

The chemical (2E)-1-(2,4-dinitrophenyl)-2-dodecylidenehydrazine, also known as DDH, is a hydrazine derivative that contains a dodecylidene chain and a 2,4-dinitrophenyl group. It has a bright yellow color and is insoluble in water, but soluble in organic solvents. DDH is commonly used as a chemical reagent for the detection and determination of aldehydes and ketones in various organic compounds. It possesses strong nucleophilic properties and is capable of forming hydrazone derivatives with carbonyl compounds. Additionally, DDH has been studied for its potential as an antibacterial and anti-cancer agent due to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1726-78-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1726-78:
(6*1)+(5*7)+(4*2)+(3*6)+(2*7)+(1*8)=89
89 % 10 = 9
So 1726-78-9 is a valid CAS Registry Number.

1726-78-9SDS

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 N-[(E)-dodecylideneamino]-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names Lauraldehyde 2,4-dinitrophenylhydrazone

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:1726-78-9 SDS

1726-78-9Downstream Products

1726-78-9Relevant articles and documents

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Lieber

, p. 2862,2864 (1949)

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AUTORECYCLING OXIDATION OF AMINES TO CARBONYL COMPOUNDS CATALYZED BY 3,4-DISUBSTITUTED 4-DEAZATOXOFLAVIN DERIVATIVES

Nagamatsu, Tomohisa,Hashiguchi, Yuko,Sakuma, Yoshiharu,Yoneda, Fumio

, p. 1309 - 1312 (2007/10/02)

3,4-Disubstituted 4-deazatoxoflavin derivatives (II) were prepared by the condensation of 6-(1-methylhydrazino)uracils (I) with appropriate α-diketones.The compounds II oxidized long-chain alkylamines such as n-octylamine and n-dodecylamine besides benzylamine and cyclohexylamine to yield the corresponding carbonyl compounds via imines, catalytically with a markedly high turnover number.

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