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606-83-7

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606-83-7 Usage

Description

3,3-Diphenylpropionic acid, also known as diphenylacetic acid, is an organic compound with the molecular formula C15H14O2. It is a white to light yellow crystalline powder that is widely used in the pharmaceutical industry for the synthesis of various drugs and compounds.

Uses

Used in Pharmaceutical Industry:
3,3-Diphenylpropionic acid is used as a key intermediate in the synthesis of steroid 5α-reductase inhibiting acylpiperidines. These compounds are known to inhibit the enzyme 5α-reductase, which plays a crucial role in the conversion of testosterone to dihydrotestosterone (DHT). Inhibiting this enzyme can help in the treatment of conditions like benign prostatic hyperplasia (BPH) and androgenetic alopecia (male pattern baldness).
Additionally, 3,3-Diphenylpropionic acid is used in the preparation of calpain-inhibitory piptidyl α-ketoacids and esters. Calpains are a family of calcium-dependent cysteine proteases that are involved in various cellular processes, including cell signaling, apoptosis, and protein turnover. Inhibiting calpains has been shown to have potential therapeutic applications in the treatment of various diseases, such as neurodegenerative disorders, muscular dystrophy, and cancer.

Synthesis Reference(s)

Journal of the American Chemical Society, 91, p. 7510, 1969 DOI: 10.1021/ja01054a049The Journal of Organic Chemistry, 39, p. 623, 1974 DOI: 10.1021/jo00919a009Tetrahedron Letters, 35, p. 1539, 1994 DOI: 10.1016/S0040-4039(00)76752-9

Purification Methods

Crystallise the acid from EtOH. [Beilstein 9 H 680.]

Check Digit Verification of cas no

The CAS Registry Mumber 606-83-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 606-83:
(5*6)+(4*0)+(3*6)+(2*8)+(1*3)=67
67 % 10 = 7
So 606-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O2/c16-15(17)11-14(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,14H,11H2,(H,16,17)

606-83-7SDS

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 3,3-Diphenylpropionic acid

1.2 Other means of identification

Product number -
Other names 3,3-diphenylpropanoic 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:606-83-7 SDS

606-83-7Relevant articles and documents

Photoredox Activation of Formate Salts: Hydrocarboxylation of Alkenes via Carboxyl Group Transfer

Huang, Yan,Hou, Jing,Zhan, Le-Wu,Zhang, Qian,Tang, Wan-Ying,Li, Bin-Dong

, p. 15004 - 15012 (2021/12/14)

A photoredox activation mode of formate salts for carboxylation was developed. Using a formate salt as the reductant, carbonyl source, and hydrogen atom transfer reagent, a wide range of alkenes can be converted into acid products via a carboxyl group tra

Covalent organic framework supported Pd(II)-catalyzed conjugate additions of arylboronic acids to α,β-unsaturated carboxylic acids

Wen, Min,Lu, Shujuan,Fan, Chaogang,Shen, Kai,Lin, Shaohui,Pan, Qinmin

, (2021/04/28)

A palladium(II)-coordinated covalent organic framework (Pd(II)@COF) was mechanochemically synthesized from [2,2′-bipyridine]-5,5′-diamine (Bpy) and 1,3,5-triformylphloroglucinol (Tp), which was demonstrated as a catalyst for conjugate addition of arylboronic acids to unreactive α,β-unsaturated carboxylic acids in aqueous media (water/acetone = 1:1). Modest to good yields were obtained for most substrates, and studies on the catalyst recyclability showed that the heterogeneous catalyst gave >80% yields in the first 4 cycles. This research broadens the application of COFs supported catalysis and gave a new option for Pd(II)-catalysis.

Synthesis method of succinic acid derivative or 3 -arylpropionic acid (by machine translation)

-

Paragraph 0101-0114; 0115; 0144, (2020/10/30)

The invention discloses a synthesis method of a succinic acid derivative or 3 -arylpropionic acid, which comprises the following steps: adding a base in a drying reaction tube and CO removing CO. 2 The reaction is carried out under the irradiation of visible light, the reaction is carried out under visible light irradiation, and then separation and purification are carried out to obtain the butanedioic acid derivative or 3 -arylpropionic acid product; the base comprises sodium tert-butoxide, potassium tert-butoxide, lithium tert-butyl alcohol and 4 - potassium carbonate; and the reaction substrate comprises an acrylate compound or an aryl vinyl compound. CO can be induced by visible light. 2 The scheme provided by the invention is mild in reaction condition and wide in reaction 3 - substrate selectivity, and the reaction substrate is wide in selectivity, the raw materials are cheap and easily available, and the method has a good industrial application prospect. (by machine translation)

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