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Benzoic acid, 2-(1-naphthyl)-2-phenylhydrazide (8CI) is a chemical compound with the molecular formula C24H20N2O2. It is a derivative of benzoic acid, where the carboxylic acid group is replaced by a hydrazide group, and the hydrazide is further substituted with a 1-naphthyl and a phenyl group. Benzoicacid, 2-(1-naphthyl)-2-phenylhydrazide (8CI) is known for its potential applications in the synthesis of various pharmaceuticals and as an intermediate in organic chemistry. It is characterized by its white crystalline appearance and is typically used in research and development settings due to its specific chemical properties and reactivity.

6295-86-9

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6295-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6295-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6295-86:
(6*6)+(5*2)+(4*9)+(3*5)+(2*8)+(1*6)=119
119 % 10 = 9
So 6295-86-9 is a valid CAS Registry Number.

6295-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(naphthalen-1-yl)-N'-phenylbenzohydrazide

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:6295-86-9 SDS

6295-86-9Downstream Products

6295-86-9Relevant academic research and scientific papers

Assembly of N, N -disubstituted hydrazines and 1-aryl-1 H-indazoles via copper-catalyzed coupling reactions

Xiong, Xiaodong,Jiang, Yongwen,Ma, Dawei

supporting information; experimental part, p. 2552 - 2555 (2012/07/13)

CuI-catalyzed coupling of N-acyl-N′-substituted hydrazines with aryl iodides takes place at 60-90 °C to afford N-acyl-N′,N′- disubstituted hydrazines regioselectively and thereby gives a facile method for assembling N,N-diaryl hydrazines. N-Acyl-N′-substituted hydrazines can also react with 2-bromoarylcarbonylic compounds at 60-125 °C under the catalysis of CuI/4-hydroxy-l-proline to provide 1-aryl-1H-indazoles.

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