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2-Propanone, 1,3-diphenyl-, phenylhydrazone is a chemical compound with the molecular formula C20H19N. It is a derivative of 2-propanone (also known as acetone), where two phenyl groups are attached to the carbonyl carbon, and a phenylhydrazone group is attached to the carbonyl oxygen. 2-Propanone, 1,3-diphenyl-, phenylhydrazone is an example of a hydrazone, which is formed by the reaction of a carbonyl compound with a hydrazine. The phenylhydrazone group in 2-Propanone, 1,3-diphenyl-, phenylhydrazone is derived from phenylhydrazine, a derivative of hydrazine with a phenyl group. 2-Propanone, 1,3-diphenyl-, phenylhydrazone is an organic compound that can be used in various chemical reactions and as an intermediate in the synthesis of other organic compounds. It is characterized by its unique structure and properties, which make it a valuable compound in the field of organic chemistry.

1788-30-3

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1788-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1788-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1788-30:
(6*1)+(5*7)+(4*8)+(3*8)+(2*3)+(1*0)=103
103 % 10 = 3
So 1788-30-3 is a valid CAS Registry Number.

1788-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name phenylhydrazone of dibenzyl ketone

1.2 Other means of identification

Product number -
Other names 1,3-Diphenyl-aceton-phenylhydrazon

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:1788-30-3 SDS

1788-30-3Relevant academic research and scientific papers

Studies on Tertiary Amine Oxides. LXXX.1) Reaction of Quinoline 1-oxide with Phenylacetic Anhydride

Funakoshi, Kazuhisa,Mizuoka, Masae,Wada, Kazuko,Saeki, Seitaro,Hamana, Masatomo

, p. 3886 - 3891 (2007/10/02)

Treatment of quinoline 1-oxide (1) with phenylacetic acid and acetic anhydride in boiling benzene for 10 h gave benzaldehyde (2), quinoline (3), 2-benzylquinoline (4), 2-benzoylquinoline (5), phenyl-di(2-quinolyl)carbinol (6), di(2-quinolyl) ketone (7), and N-(2-quinolyl)-2-benzylidene-1,2-dihydroquinoline (8) in small yields.The reaction of 1 with phenylacetic anhydride in boiling benzene for 10 h afforded 1,3-diphenyl-1-(2-quinolyl)acetone (9) and dibenzyl ketone (10) together with small amounts of 2, 3, and 5.Further, it was found that phenylacetic anhydrideundergoes decarboxylative coupling upon heating with tertiary amines to give 10.The mechamisms of these reactions are discussed. Keywords --- nucleophilic reaction; oxidative decarboxylation; decarboxylative coupling; benzaldehyde; 2-benzylquinoline; phenyl-di(2-quinolyl)carbinol; N-(2-quinolyl)-2-benzylidene-1,2-dihydroquinoline; 1,3-diphenyl-1-(2-quinolyl)acetone; dibenzyl ketone

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