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1567-38-0

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1567-38-0 Usage

General Description

(1E)-1,2-diphenylethanone semicarbazone is a chemical compound with the molecular formula C15H15N3O. It is a semicarbazone derivative of 1,2-diphenylethanone and is often used in organic chemistry as a reagent for the determination of carbonyl compounds. (1E)-1,2-diphenylethanone semicarbazone has a notable yellow color and can be crystallized from various solvents. It is also known for its potential applications in the field of medicine and biochemistry, particularly in the study of the structure and function of certain enzymes and proteins. Additionally, (1E)-1,2-diphenylethanone semicarbazone is classified as a moderate hazard chemical, with potential risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1567-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1567-38:
(6*1)+(5*5)+(4*6)+(3*7)+(2*3)+(1*8)=90
90 % 10 = 0
So 1567-38-0 is a valid CAS Registry Number.

1567-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-1,2-diphenylethylideneamino]urea

1.2 Other means of identification

Product number -
Other names 1,4-dihydro-2,6-dimethyl-4-phenyl-3,5-pyridinecarboxylic acid dimethyl ester

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:1567-38-0 SDS

1567-38-0Relevant articles and documents

Reaction of Substituted Hydrazones with Thionyl Chloride and Sulfuryl Chloride

Meier, Herbert,Trickes, Georg,Laping, Elisabeth,Merkle, Ursula

, p. 183 - 192 (2007/10/02)

Treatment of acetylhydrazones 2, ethoxycarbonylhydrazones 3, p-tolylsulfonylhydrazones 4 or semicarbazones 5 with thionyl chloride leads to the 1,2,3-thiadiazoles 6a-o.Sulfuryl chloride on the other hand accomplishes the transfer of chlorine without incorporating a sulfur atom.The new synthesized 1,2,3-thiadiazoles 6g-o are characterized in detail by spectroscopic methods.

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