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63413-91-2

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63413-91-2 Usage

Description

3-(Phenylthio)acrylic acid, also known as cis-β-phenyl thioacrylic acid, is an organic compound with the molecular formula C?H?OS. It is characterized by the presence of a phenyl group (C?H?) attached to a thioacrylic acid moiety (C?H?OS). The ionization constants of cis-β-phenyl thioacrylic acid and its ring derivatives have been evaluated, indicating its potential reactivity and applications in various fields.

Uses

Used in Chemical Synthesis:
3-(Phenylthio)acrylic acid is used as a building block in the synthesis of various organic compounds, particularly those involving the phenylthio group. Its unique structure allows for the formation of new molecules with potential applications in pharmaceuticals, materials science, and other industries.
Used in Pharmaceutical Industry:
3-(Phenylthio)acrylic acid is used as an intermediate in the development of pharmaceutical compounds. Its ability to form various derivatives makes it a valuable component in the design and synthesis of new drugs with potential therapeutic properties.
Used in Materials Science:
3-(Phenylthio)acrylic acid is used as a component in the development of novel materials with specific properties, such as optical, electronic, or mechanical characteristics. Its incorporation into polymers or other materials can lead to the creation of advanced materials with applications in various industries.
Used in Research and Development:
3-(Phenylthio)acrylic acid is used as a research compound for studying its chemical properties, reactivity, and potential applications in various fields. Its unique structure and the ability to form derivatives make it an interesting subject for scientific investigation and the development of new technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 63413-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,1 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63413-91:
(7*6)+(6*3)+(5*4)+(4*1)+(3*3)+(2*9)+(1*1)=112
112 % 10 = 2
So 63413-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O2S/c10-9(11)6-7-12-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+

63413-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-phenylsulfanylprop-2-enoic acid

1.2 Other means of identification

Product number -
Other names HMS1737K20

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:63413-91-2 SDS

63413-91-2Relevant articles and documents

Sulfonium Ylides by (3+2) Cycloaddition of Arynes with Vinyl Sulfides: Stereoselective Synthesis of Highly Substituted Alkenes

Li, Yuanming,Mück-Lichtenfeld, Christian,Studer, Armido

supporting information, p. 14435 - 14438 (2016/11/11)

The reaction of in situ generated arynes with vinyl sulfides provides benzannulated sulfonium ylides in a (3+2) cycloaddition. Trapping of the intermediate ylides with electrophiles (proton transfer or a second aryne addition) and subsequent β-elimination give rise to di-, tri-, or tetrasubstituted alkenes with high stereoselectivity. Experimental studies and DFT calculations provide insight into the mechanisms of these cascade reactions.

Organylzinc Chalcogenolate Promoted Michael-Type Addition of α,β-Unsaturated Carbonyl Compounds

L?ren Nunes, Vanessa,De Oliveira, Ingryd Cristina,Soares Do Rêgo Barros, Olga

supporting information, p. 1525 - 1530 (2015/10/05)

We present the chemo-, regio-, and stereoselective synthesis of vinyl chalcogenide compounds promoted by organylzinc chalcogenolates. In this protocol, reductive cleavage of diorganyl dichalcogenide bonds by the Zn/NH4OH system led to organylzi

DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS

-

Paragraph 0989; 0990, (2013/04/10)

The invention relates to inhibitors of the phosphodiesterase 4 (PDE4) enzyme. More particularly, the invention relates to compounds that are derivatives of 1-phenyl-2-pyridinyl alkyl alcohols, methods of preparing such compounds, compositions containing them and therapeutic use thereof.

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