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3-oxo-4-(phenylhydrazono)-3,4-dihydronaphthalene-2-carboxamide is a complex organic compound with the molecular formula C18H15N3O2. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a carbonyl group (C=O) at the 3-position, a phenylhydrazone group at the 4-position, and a carboxamide group at the 2-position. 3-oxo-4-(phenylhydrazono)-3,4-dihydronaphthalene-2-carboxamide is characterized by its conjugated π-electron system, which contributes to its stability and reactivity. It is synthesized through a series of chemical reactions, including the formation of the dihydronaphthalene core, followed by oxidation and subsequent reaction with phenylhydrazine to form the phenylhydrazone group. The carboxamide group is introduced in a later step, providing the compound with its unique structure. 3-oxo-4-(phenylhydrazono)-3,4-dihydronaphthalene-2-carboxamide is of interest in organic chemistry due to its potential applications in the synthesis of pharmaceuticals and other specialty chemicals, as well as its role as a precursor in the preparation of more complex molecules.

6268-37-7

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6268-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6268-37-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6268-37:
(6*6)+(5*2)+(4*6)+(3*8)+(2*3)+(1*7)=107
107 % 10 = 7
So 6268-37-7 is a valid CAS Registry Number.

6268-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-3-chloroprop-2-enyl]benzene

1.2 Other means of identification

Product number -
Other names 1-phenylallyl chloride

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:6268-37-7 SDS

6268-37-7Relevant academic research and scientific papers

Application of Phase Transfer Catalysis, 14.- Preparation of Alkynes from Halides with Solid Potassium tert-Butoxide and Crown Ether

Dehmlow, Eckehard V.,Lissel, Manfred

, p. 1 - 13 (2007/10/02)

Preparatively very simple and mild HX eliminations with solid potassium tert-butoxide in petroleum ether in the presence of catalytic amounts of crown-6 are described. 1,2-Dihalides (from alkenes) and 1,1-dihalides (from aldehydes) yield 1-alkynes; internal geminal dihalides (from symmetric ketones) give internal alkynes in excellent yields. 2,2-Dihalides (from methyl ketones) yield homogeneous 1-alkynes only if the 3-position is blocked. (E)-Haloalkenes lead also to alkynes in a syn-elimination process.

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