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Benzaldehyde Methylphenylhydrazone (BMPH) is an organic compound with the chemical formula C14H14N2. It is formed by the reaction of benzaldehyde with methylphenylhydrazine, resulting in a yellow crystalline solid. BMPH is commonly used as a derivatization agent in analytical chemistry, particularly for the detection and quantification of aldehydes and ketones. It is also employed as a ligand in coordination chemistry and has potential applications in the synthesis of pharmaceuticals and agrochemicals. The compound is known for its stability and solubility in various solvents, making it a valuable tool in research and industry.

2989-45-9

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2989-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2989-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2989-45:
(6*2)+(5*9)+(4*8)+(3*9)+(2*4)+(1*5)=129
129 % 10 = 9
So 2989-45-9 is a valid CAS Registry Number.

2989-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-phenylhydrazone of benzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde N-methyl-N-phenylhydrazone

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:2989-45-9 SDS

2989-45-9Relevant academic research and scientific papers

Synthesis of o -(dimethylamino)aryl ketones, acridones, acridinium salts, and 1 H -indazoles by the reaction of hydrazones and arynes

Dubrovskiy, Anton V.,Larock, Richard C.

, p. 11232 - 11256 (2013/02/23)

A novel, efficient route to biologically and pharmaceutically important o-(dimethylamino)aryl ketones, acridones, acridinium salts, and 1H-indazoles has been developed starting from readily available hydrazones of aldehydes and o-(trimethylsilyl)aryl triflates. The reaction proceeds through arynes under mild conditions, tolerates a wide range of functional groups, and provides the final products in good to excellent yields.

Photoinduced cleavage of N-N bonds of aromatic hydrazines and hydrazides by visible light

Zhu, Mingzhao,Zheng, Nan

experimental part, p. 2223 - 2236 (2011/09/15)

A photocatalytic system involving [Ru(bpyrz)(PFH, visible light, and air has been developed for cleavage of the N-N bonds of hydrazines and hydrazides. This catalytic system is generally effective for N,N-disubstituted hydrazine and hydrazide derivatives, including arylhydrazides, N-alkyl-N-arylhydrazines, and N,N-diarylhydrazines. The utility of this cleavage reaction has been demonstrated by synthesizing a variety of secondary aromatic amines. Georg Thieme Verlag Stuttgart ? New York.

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