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2-Propen-1-one, 3-phenyl-1-[2-(phenylmethoxy)phenyl]-, also known as 3-phenyl-1-[2-(phenylmethoxy)phenyl]-2-propen-1-one, is a complex organic compound with the molecular formula C20H16O2. It is a derivative of 2-propen-1-one, featuring a phenyl group at the 3-position and a phenylmethoxyphenyl group at the 1-position. 2-Propen-1-one, 3-phenyl-1-[2-(phenylmethoxy)phenyl]- is characterized by its conjugated double bonds and aromatic rings, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. Due to its specific structure, it may exhibit unique properties and reactivity compared to simpler alkenes and ketones, making it a subject of interest for chemical research and development.

4537-31-9

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4537-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4537-31-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,3 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4537-31:
(6*4)+(5*5)+(4*3)+(3*7)+(2*3)+(1*1)=89
89 % 10 = 9
So 4537-31-9 is a valid CAS Registry Number.

4537-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-benzyloxyphenyl)-3-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names (E)-1-(2-Benzyloxy-phenyl)-3-phenyl-propenone

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:4537-31-9 SDS

4537-31-9Relevant academic research and scientific papers

Electrochemical 1,4-reduction of α,β-unsaturated ketones with methanol and ammonium chloride as hydrogen sources

Huang, Binbin,Li, Yanan,Yang, Chao,Xia, Wujiong

supporting information, p. 6731 - 6734 (2019/06/17)

A sustainable, chemoselective 1,4-reduction of α,β-unsaturated ketones by means of an electrochemical method is presented, wherein the extremely inexpensive ammonium chloride (NH4Cl) is applied as the only additive. The reaction proceeds smoothly in the air at ambient temperature. Mechanistic studies reveal that both NH4Cl and solvent methanol work as hydrogen donors.

ALLOSTERIC PROTEIN KINASE MODULATORS

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Page/Page column 52, (2012/03/10)

The invention provides specific small molecule compounds that allosterically regulate the activity or modulate protein-protein interactions of AGC protein kinases and the Aurora family of protein kinases, methods for their production, pharmaceutical compositions comprising same, and their use for preparing medicaments for the treatment and prevention of diseases related to abnormal activities of AGC protein kinases or of protein kinases of the Aurora family.

ALLOSTERIC PROTEIN KINASE MODULATORS

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Page/Page column 107, (2010/04/30)

The invention provides specific small molecule compounds that allosterically regulate the activity or modulate protein-protein interactions of AGC protein kinases and the Aurora family of protein kinases, methods for their production, pharmaceutical compositions comprising same, and their use for preparing medicaments for the treatment and prevention of diseases related to abnormal activities of AGC protein kinases or of protein kinases of the Aurora family.

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