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2-hydroxy-2-(4-methylphenyl)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70589-40-1

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70589-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70589-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,8 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70589-40:
(7*7)+(6*0)+(5*5)+(4*8)+(3*9)+(2*4)+(1*0)=141
141 % 10 = 1
So 70589-40-1 is a valid CAS Registry Number.

70589-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name α-tolyl-α-hydroxypropionic acid

1.2 Other means of identification

Product number -
Other names 2-hydroxy-2-p-tolyl-propionic 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:70589-40-1 SDS

70589-40-1Relevant academic research and scientific papers

Synthesis of α-hydroxycarboxylic acids from various aldehydes and ketones by direct electrocarboxylation: A facile, efficient and atom economy protocol

Singh, Kishanpal,Sohal, Harvinder Singh,Singh, Baljit

, p. 839 - 845 (2021/04/09)

In present work, the formation of α-hydroxycarboxylic acids have been described from various aromatic aldehydes and ketones via direct electrocarboxylation method with 80-92% of yield without any side product and can be purified by simple recrystallization using sacrificial Mg anode and Pt cathode in an undivided cell, CO2at (1 atm) was continuously bubbled in the cell throughout the reaction using tetrapropylammonium chloride as a supporting electrolyte in acetonitrile. The synthesized compounds obtained in fair to excellent yield with a high level of purity. The characterization of electrocarboxylated compounds was done with spectroscopic techniques like IR, NMR (1H & 13C), mass and elemental analysis.

Facile one-pot preparation of 2-arylpropionic and arylacetic acids from cyanohydrins by treatment with aqueous HI

Aramini, Andrea,Sablone, Manolo R.,Bianchini, Gianluca,Amore, Alessia,Fanì, Michela,Perrone, Plinio,Dolce, Alberto,Allegretti, Marcello

experimental part, p. 2015 - 2021 (2009/07/04)

A novel one-pot two-step procedure has been developed to synthesize highly substituted 2-arylpropionic and arylacetic acids, by treatment with aqueous HI, from cyanohydrins. The hydrogenolytic reduction of α-hydroxy-2-arylpropionic acids was the key step of the process and the optimization of the reaction conditions led to identify aqueous HI as an appropriate and selective reagent for the reductive deoxygenation of cyanohydrins. The synthetic route described a general and efficient strategy for the preparation of large libraries of phenylacetic and phenylpropionic acids derivatives.

A new method for the preparation of 2-aryl propionic acids using low-valent titanium

Garcia, Mariano,Del Campo, Carmen,Sinisterra, Jose V.,Llama, Emilio F.

, p. 7973 - 7974 (2007/10/02)

The addition of dihalocarbenes to arylmethylketones in the presence of low-valent titanium yields 2-aryl propionic acids in acceptable yield by one pot reaction. The reaction conditions were optimized. The TiCl4/LiAlH4 ratio is one variable that controls the selectivity of the process.

Chemoenzymatic synthesis of pure enantiomeric 2-aryl propionic acids

Garcia,Del Campo,Llama,Sanchez-Montero,Sinisterra

, p. 8433 - 8440 (2007/10/02)

A new chemoenzymatic procedure to obtain pure enantiomeric 2-arylpropionic acids is described. The one pot synthesis of (±)-2-arylpropionic acids is carried out by addition of dichlorocarbene to the C=O bond of arylmethylketones and hydrogenolysis of the additon product. The racemic mixture is resolved by enantiospecific hydrolysis of the racemic ethyl esters using native lipase from Candida rugosa. The good yields, the accessibility of the starting arylmethylketones and the stereospecificity of the enzymatic hydrolysis make the process interesting in order to obtain the same non steroidal antiinflammatory drugs such as Ibuprofen or Naproxen.

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