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(E)-1-phenyl-2-[(Z)-(2-phenylhydrazinylidene)methyl]diazene is a complex organic compound characterized by a phenyl group attached to a diazene moiety, which features a double bond between the nitrogen atoms. The compound has a Z-configuration, indicating that the substituents on the double bond are arranged in a specific geometric pattern, with the phenyl group and the hydrazinylidene group on the same side of the double bond. This molecule is of interest in organic chemistry due to its unique structure and potential applications in the synthesis of pharmaceuticals and other chemical compounds.

1885-34-3

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1885-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1885-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1885-34:
(6*1)+(5*8)+(4*8)+(3*5)+(2*3)+(1*4)=103
103 % 10 = 3
So 1885-34-3 is a valid CAS Registry Number.

1885-34-3SDS

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 Diphenyl formazan

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

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More Details:1885-34-3 SDS

1885-34-3Relevant academic research and scientific papers

OXIDES OF 3-METHYL-1,2,4-BENZOTRIAZINE

Atallah, Raja H.,Nazer, Musa Z.

, p. 1793 - 1796 (2007/10/02)

The previously prepared 3-methyl-1,2,4-benzotriazine oxide is shown to be the 4-oxide 5.Synthesis and structores of other isomeric and related oxides are described.A modification of a previously described synthesis of 1,2,4-benzotriazines produces purer products in higher yields.

INVESTIGATIONS IN THE SERIES OF ARYLHYDRAZONES OF SUBSTITUTED GLYOXYLIC ACIDS. XXVI. REACTION OF ETHYL CYANOPYRUVATE WITH ARENEDIAZONIUM SALTS

Dubenko, R. G.,Konysheva, V. D.,Pel'kis, P. S.

, p. 751 - 757 (2007/10/02)

Ethyl sodiocyanopyruvate reacts with arenediazonium salts in a neutral medium (pH ca. 7) to form ethoxalylglyoxylonitrile arylhydrazones.The action of 15percent aqueous alkali or small amounts of sulfuric acid on the ethoxalylglyoxylonitrile arylhydrazone

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