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Propanoic acid, 3-[(phenylmethyl)sulfinyl]-, also known as 3-(benzylsulfinyl)propanoic acid, is an organic compound with the chemical formula C10H12O3S. It is a derivative of propanoic acid, featuring a phenylmethyl sulfoxide group attached to the third carbon. Propanoic acid, 3-[(phenylmethyl)sulfinyl]- is characterized by its molecular weight of 216.27 g/mol and a melting point of 65-67°C. It is a colorless to pale yellow solid and is soluble in organic solvents. This chemical is primarily used in the synthesis of pharmaceuticals and other organic compounds, particularly in the preparation of chiral auxiliaries and ligands in asymmetric catalysis. Due to its reactivity and functional group diversity, it plays a significant role in the field of organic chemistry and drug development.

6058-80-6

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6058-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6058-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6058-80:
(6*6)+(5*0)+(4*5)+(3*8)+(2*8)+(1*0)=96
96 % 10 = 6
So 6058-80-6 is a valid CAS Registry Number.

6058-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzylsulfinylpropanoic acid

1.2 Other means of identification

Product number -
Other names 3-phenylmethanesulfinyl-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:6058-80-6 SDS

6058-80-6Relevant academic research and scientific papers

Selective Catalytic Oxidation of Organic Sulfides to Sulfoxides without Forming Sulfones over Solid Molybdenum Blue: Kinetic and Thermodynamic Studies

Ratheshkumar,Induja,Raghavan

, p. 2267 - 2274 (2020/09/16)

The present investigation reports studies on the selective catalytic oxidation of organic sulfide substrates over molybdenum blue catalyst supported on boron phosphate. The catalyst was synthesized through partial precipitation method and characterized by

Asymmetric sulfoxidation catalyzed by a vanadium bromoperoxidase: Substrate requirements of the catalyst

Andersson, Malin A.,Allenmark, Stig G.

, p. 15293 - 15304 (2007/10/03)

An investigation of the catalytic effect of vanadium bromoperoxidase (VBrPO, from Corallina officinalis) on the oxidation of a series of prochiral sulfides by hydrogen peroxide, revealed that substrates having a cis- positioned carboxyl group are oxidized

Cis-platinum complexes with chelating amines and sulphinyl carboxylates

-

, (2008/06/13)

STR1 Platinum (II) complexes of formula (I) where: Am is a monodentate amine, or (Am)2 is a bidentate amine, B represents a straight or branched alkyl residue or a single bond, R is selected from the group of hydrogen, (C3 -C8) cycloalkyl, phenyl or naphthyl which may be substituted by halogens (I, Br, Cl, F), trihalomethane, hydroxyl, (C1 -C4)-alkoxyl, (C1 -C7)-acylamino, (C1 -C7)-sulphamido, allyl, phenoxyl, haloalkoxyl, nitro, cyano, azido, with condition that when R is hydrogen B is different from a single bond, Q is a residue of formula --(CH2)n1 --CRa Rb --(CH2)n2 --, 1,2- or 2,3-naphthalene, benzo-1,3-dioxolan-5,6-diyl, substituted or unsubstituted 1,2-phenylene, Ra and Rb are selected independently of each other from the group of hydrogen, allyl, linear or branched (C1 -C8)-alkyl, --(CH2)p OH, --(CH2 CH2 O)q --CH3, or taken together with the carbon atom to which they are bonded form a (C3 -C8) cycloalkyl, or heterocyclic tetrahydropyran-4,4-diyl, n1 and n2 are independently zero or the integer 1, p is an integer from 2 to 6, and q is an integer from 1-3, X- is a biocompatible anion such as chloride, bromide, iodide, nitrate, perchlorate, or one equivalent of sulphate or phosphate, or an anion of a monovalent C1 -C4 organic acid such as acetate, propionate or chloroacetate, or of an aromatic acid such as benzoate, or of a heteroaromatic acid such as nicotinate are described. The compounds are useful as anti-tumor drugs.

GOLD(III) CATALYZED OXIDATION OF SULFIDES TO SULFOXIDES BY NITRIC ACID UNDER PHASE-TRANSFER CONDITIONS: A NEW SYNTHESIS OF SULFOXIDES

Gasparrini, F.,Giovannoli, M.,Misiti, D.,Natile, G.,Palmieri, G.

, p. 3181 - 3184 (2007/10/02)

Gold(III) halides catalyze the oxidation of sulfides to sulfoxides in a phase-transfer process.The organic sulfides, dissolved in nitromethane, are treated with (Bu4N(1+)*AuCl4(1-)) in catalytic amount and aqueous nitric acid wich acts as an oxidant.The oxidation of the thio-group is selective and can be carried out also in the presence of other oxidizable groups, such as vinyl, tertiary amino, hydroxy, diol etc, which are left unchanged.Moreover in the case of asymmetric disulfides the reaction is regiospecific leading to the fomation of a single monosulfoxide.

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