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10569-35-4

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10569-35-4 Usage

General Description

2-Phenyl-3-(2-thienyl)acrylic acid is a chemical compound characterized by a phenyl ring and a thiophene ring connected through an acrylic acid chain. The compound has distinctive aromatic properties due to the presence of the phenyl and thiophene rings, and features conjugated unsaturated bonds, which may contribute to its potential reactivity. The compound's properties might allow it to have uses in various fields such as organic synthesis, pharmaceuticals, and material sciences. However, precise information about its specific applications, safety profile, and detailed physicochemical properties are scarce and would require more specific research.

Check Digit Verification of cas no

The CAS Registry Mumber 10569-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10569-35:
(7*1)+(6*0)+(5*5)+(4*6)+(3*9)+(2*3)+(1*5)=94
94 % 10 = 4
So 10569-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O2S/c14-13(15)12(9-11-7-4-8-16-11)10-5-2-1-3-6-10/h1-9H,(H,14,15)/p-1

10569-35-4SDS

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 2-phenyl-3-(2-thienyl)acrylic acid

1.2 Other means of identification

Product number -
Other names 2-phenyl-3-thiophen-2-yl-acrylic 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:10569-35-4 SDS

10569-35-4Relevant articles and documents

CH?S hydrogen bonds as the organising force in 2,3-thienyl- and phenyl- or 2,3-dithienyl-substituted propenoic acid aggregates studied by the combination of FT-IR spectroscopy and computations

Csankó,Illés,Felf?ldi,Kiss,Sipos,Pálinkó

experimental part, p. 259 - 263 (2011/06/27)

Various propenoic acid stereoisomers 2,3-disubstituted with thienyl and/or phenyl groups were synthesised and their aggregation behaviour was studied both in solution and in the solid state by experimental (mid-range FT-IR spectroscopy) and computational

SYNTHESIS OF (5-STYRYL-2-THIENYL)-PHENYLACRYLIC ACIDS

Karminski-Zamola, Grace,Bajic, Miro

, p. 1497 - 1501 (2007/10/02)

We describe the synthesis of E-3-(5-styryl-2-thienyl)-2-phenylacrylic acid 7, E-3-(5-styryl-2-thienyl)-2-(4-methoxyphenyl)acrylic acid 8, E-3--2-phenylacrylic acid 9 and E-3--2-(4

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