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2,3,4-Triphenylbutanoic acid is a synthetic organic compound with the chemical formula C26H22O2. It is a white crystalline solid that is soluble in organic solvents. 2,3,4-triphenylbutanoic acid is characterized by the presence of three phenyl rings attached to a butanoic acid backbone, with the phenyl groups positioned at the 2nd, 3rd, and 4th carbon atoms. It is used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The compound is also known for its potential applications in materials science and as a ligand in coordination chemistry. Its synthesis typically involves the Friedel-Crafts acylation of triphenylmethane with acetyl chloride, followed by hydrolysis to yield the carboxylic acid.

5468-20-2

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5468-20-2 Usage

Physical form

White to off-white crystalline powder

Solubility

Sparingly soluble in water

Primary use

Synthesis of various pharmaceuticals and fine chemicals

Secondary use

Intermediate in the production of fragrances and other organic compounds

Role in chemical research

Chiral auxiliary in asymmetric synthesis

Potential applications

Organic electronics and materials science due to unique molecular structure

Check Digit Verification of cas no

The CAS Registry Mumber 5468-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5468-20:
(6*5)+(5*4)+(4*6)+(3*8)+(2*2)+(1*0)=102
102 % 10 = 2
So 5468-20-2 is a valid CAS Registry Number.

5468-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4-triphenylbutanoic acid

1.2 Other means of identification

Product number -
Other names 1,2,3-triphenylbutyric acid

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:5468-20-2 SDS

5468-20-2Relevant academic research and scientific papers

Interesting reactivity in the thermolysis and photolysis of 2,3-diphenyl-1-naphthol

Guzei, Ilia A.,Zimmerman, Howard E.,Shorunov, Sergey,Spencer, Lara C.

experimental part, p. 399 - 406 (2010/04/06)

2,3-Diphenyl-1-naphthol (1) undergoes two unexpected reactions under different conditions. Compound (1) was heated in DMSO-d6 and underwent a Pummerer type thermal reaction to give two isomeric products, 1-(methylthio)methoxy-2,3-diphenyl naphthol-d5 which crystallized in the space group P1 with a = 7.1610(9) A, b = 11.2795(15) A, c = 12.8905(17) A, α = 114.049(2)°, β = 96.589(2)°, and γ = 102.945(2)°, and 2-(methylthio)methyl-2,3-diphenyl 1(2H)-naphthalenone-d5 which crystallized in the space group P1 with a = 8.5981(5) A, b = 10.4374(6) A, c = 11.1078(6) A, α = 78.748(2)°, β = 67.709(2)°, and γ = 83.184(2)°. Photolysis (254 nm) of (1) resulted in 2,2',3,3'-tetraphenyl-1,1'-bi-2-naphthol which crystallized in the space group P21/c with a = 26.3616(11) A, b = 10.1707(4) A, c = 23.3376(9) A, and β = 99.034(2)°.

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