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1-[4-(4-propanoylphenyl)phenyl]propan-1-one is a complex organic compound with the molecular formula C18H18O2. It is a derivative of acetophenone, featuring a propanoyl group (a three-carbon chain with a carboxylic acid group) attached to a phenyl ring. The structure consists of a propane-1-one backbone with two phenyl groups, one of which is further substituted with a propanoyl group. 1-[4-(4-propanoylphenyl)phenyl]propan-1-one is characterized by its aromatic properties and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure. However, specific applications and properties would require further investigation and characterization.

4392-77-2

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4392-77-2 Usage

Molar mass

250.34 g/mol

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Functional group

Ketone

Derivative of

Acetophenone

Physical appearance

White to off-white crystalline powder

Solubility in water

Sparingly soluble

Solubility in organic solvents

Soluble in ethanol and ether

Specific applications

Depend on the industry and chemical processes in which it is used

Check Digit Verification of cas no

The CAS Registry Mumber 4392-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4392-77:
(6*4)+(5*3)+(4*9)+(3*2)+(2*7)+(1*7)=102
102 % 10 = 2
So 4392-77-2 is a valid CAS Registry Number.

4392-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(4-propanoylphenyl)phenyl]propan-1-one

1.2 Other means of identification

Product number -
Other names Bis-(4-propionylphenyl)

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:4392-77-2 SDS

4392-77-2Upstream product

4392-77-2Downstream Products

4392-77-2Relevant academic research and scientific papers

Amphiphilic viologen: Electrochemical generation of organic reductant and pd-catalyzed reductive coupling of aryl halides in water

Kuroboshi, Manabu,Yamamoto, Takashi,Tanaka, Hideo

, p. 197 - 200 (2013)

Electroreduction of 1,1′-bis(methoxyethoxyethoxyethyl)-4,4′- bipyridinium tosylate generated amphiphilic organic reductants, which promoted the Pd-catalyzed reductive coupling of aryl bromides in water to give the corresponding biaryls. The yields and selectivity of biaryls depended on the length of ethyleneoxy groups and substituents of the aryl bromides. Georg Thieme Verlag Stuttgart · New York.

Viologen as catalytic organic reductant: Electro-reductive dimerization of aryl bromides in a Pd/viologen double mediatory system

Kuroboshi, Manabu,Shiba, Takuya,Tanaka, Hideo

, p. 3666 - 3668 (2013/07/05)

Viologen can be used as an in situ recyclable organic reductant. Pd-catalyzed electrochemical reductive coupling of aryl bromides was performed by using a catalytic amount of viologen to afford the corresponding biaryls in good to moderate yields.

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