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Phenoxy(phenyl)acetic acid, with the molecular formula C14H12O3, is a white solid chemical compound that is slightly soluble in water. It serves as a versatile precursor in the synthesis of a range of pharmaceuticals, including diuretics and antihistamines, and is also utilized in the production of dyes, perfumes, and other organic compounds. Its potential applications extend to the chemical industry as a building block for the synthesis of various organic compounds, and it has been investigated for its biological and pharmacological properties, such as anti-inflammatory and antioxidant effects.

3117-38-2

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3117-38-2 Usage

Uses

Used in Pharmaceutical Industry:
Phenoxy(phenyl)acetic acid is used as a precursor in the synthesis of various pharmaceuticals, such as diuretics and antihistamines, due to its ability to serve as a building block for the development of these medications.
Used in Dye and Perfume Industry:
Phenoxy(phenyl)acetic acid is used as a starting material in the production of dyes and perfumes, contributing to the creation of a variety of colorants and fragrances.
Used in Chemical Industry:
Phenoxy(phenyl)acetic acid is used as a building block in the synthesis of various organic compounds, highlighting its importance in the chemical industry for creating a wide array of products.
Used in Research and Development:
Phenoxy(phenyl)acetic acid is studied for its potential biological and pharmacological properties, such as anti-inflammatory and antioxidant effects, which may lead to the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 3117-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3117-38:
(6*3)+(5*1)+(4*1)+(3*7)+(2*3)+(1*8)=62
62 % 10 = 2
So 3117-38-2 is a valid CAS Registry Number.

3117-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenoxy-2-phenylacetic acid

1.2 Other means of identification

Product number -
Other names ACETIC ACID,PHENOXYPHENYL

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:3117-38-2 SDS

3117-38-2Relevant academic research and scientific papers

CARBOXYLIC ACID DERIVATIVE AS AT2R RECEPTOR ANTAGONIST

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Paragraph 0104; 0106, (2020/03/24)

The present invention relates to a compound shown in formula (II) or a pharmaceutically acceptable salt thereof and an application of the same in preparing a drug for treating a disease related to angiotensin II receptor type 2 (AT2R).(II)

Access to Optically Enriched α-Aryloxycarboxylic Esters via Carbene-Catalyzed Dynamic Kinetic Resolution and Transesterification

Liu, Bin,Song, Runjiang,Xu, Jun,Majhi, Pankaj Kumar,Yang, Xing,Yang, Song,Jin, Zhichao,Chi, Yonggui Robin

supporting information, p. 3335 - 3338 (2020/04/30)

Optically active α-aryloxycarboxylic acids and their derivatives are important functional molecules. Disclosed here is a carbene-catalyzed dynamic kinetic resolution and transesterification reaction for access to this class of molecules with up to 99% yields and 99:1 er values. Addition of a chiral carbene catalyst to the ester substrate leads to two diastereomeric azolium ester intermediates that can quickly epimerize to each other and thus allows for effective dynamic kinetic resolution to be realized. The optically enriched ester products from our reaction can be quickly transformed to chiral herbicides and other bioactive molecules.

Highly Enantioselective Hydrogenation of Amides via Dynamic Kinetic Resolution Under Low Pressure and Room Temperature

Rasu, Loorthuraja,John, Jeremy M.,Stephenson, Elanna,Endean, Riley,Kalapugama, Suneth,Clément, Roxanne,Bergens, Steven H.

, p. 3065 - 3071 (2017/03/11)

High-throughput screening and lab-scale optimization were combined to develop the catalytic system trans-RuCl2((S,S)-skewphos)((R,R)-dpen), 2-PrONa, and 2-PrOH. This system hydrogenates functionalized α-phenoxy and related amides at room temperature under 4 atm H2 pressure to give chiral alcohols with up to 99% yield and in greater than 99% enantiomeric excess via dynamic kinetic resolution.

Potential antidepressant agents. α-Aryloxy-benzyl derivatives of ethanolamine and morpholine

Melloni,Carniel,Della Torre,et al.

, p. 235 - 242 (2007/10/02)

Various α-aryloxy-benzyl derivatives of ethanolamine and morpholine were synthesized and tested as potential antidepressant agents. A morpholine derivative, the 2-[α-(2-ethoxy-phenoxy) benzyl]morpholine, showed outstanding activity in the antireserpine te

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