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2-Propenoic acid, 3-(4-sulfophenyl)-, also known as 3-(4-sulfophenyl)acrylic acid or 4-sulfophenyl acrylic acid, is an organic compound characterized by the presence of a sulfonic acid group attached to a phenyl ring, which is in turn connected to an acrylic acid moiety. This molecule has a molecular formula of C9H8O5S and a molecular weight of 236.22 g/mol. It is a colorless to pale yellow crystalline solid that is soluble in water and has a melting point of approximately 200°C. This chemical is primarily used in the synthesis of dyes, pharmaceuticals, and other specialty chemicals due to its unique reactivity and functional groups. It is also known for its potential applications in the preparation of polymers and as a building block in the chemical industry.

13586-83-9

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13586-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13586-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,8 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13586-83:
(7*1)+(6*3)+(5*5)+(4*8)+(3*6)+(2*8)+(1*3)=119
119 % 10 = 9
So 13586-83-9 is a valid CAS Registry Number.

13586-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-sulfophenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 4-sulfo-cinnamic 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:13586-83-9 SDS

13586-83-9Relevant academic research and scientific papers

Iron(ii) coordination pyrazole complexes with aromatic sulfonate ligands: The role of ether

Kumar, Varun,El-Massaoudi, Mohamed,Radi, Smaail,Van Hecke, Kristof,Rotaru, Aurelian,Garcia, Yann

, p. 13902 - 13912 (2020)

Four novel heteroleptic mononuclear Fe(ii) coordination complexes including 3,5-dimethyl-1-(2′-pyridyl)-pyrazole (DMPP) and aromatic sulfonate ligands were synthesized and characterized using single crystal-XRD, SQUID magnetometry and 57Fe M?ssbauer spectroscopy. The crystal structures of the complexes revealed the unusual coordination of sulfonate groups to Fe(ii) ions, leading to an Fe-N4O2 coordination environment. This specific molecular layout is presumably caused by diethyl ether, which was vapour diffused into the complexation medium to obtain crystalline complexes. Alongside yielding single crystals, diethyl ether also altered the self-assembly process of a usual FeN6 homoleptic coordination environment. All the complexes remain paramagnetic at all temperatures as suggested by magnetic susceptibility measurements. All are stable in air except [Fe(DMPP)2(tos)2] which got partially oxidized to Fe(iii) over time as suggested by 57Fe M?ssbauer spectroscopy. This journal is

8-(Sulfostyryl)xanthines: Water-soluble A(2A)-selective adenosine receptor antagonists

Mueller, Christa E.,Sandoval-Ramirez, Jesus,Schobert, Ulrike,Geis, Uli,Frobenius, Wolfram,Klotz, Karl-Norbert

, p. 707 - 719 (2007/10/03)

8-(Sulfostyryl)xanthine derivatives were synthesized as water-soluble A(2A)-selective adenosine receptor (AR) antagonists. meta- and para-sulfostyryl-DMPX (3,7-dimethyl-1-propargylxanthine) derivatives 11a and 11b exhibited high affinity to rat A(2A)-AR in submicromolar concentrations, and were 20- to 30-fold selective versus rat A1-AR. Styryl-DMPX derivatives were inactive at human A(2B)- and A3-AR. 1,3-Dipropyl-8-p-sulfostyrylxanthine (13) and its 7-methyl derivative (14) showed similar (13) or higher (14) A(2A) affinity than 11a and 11b but showed no (13) or only a low degree (14) of selectivity versus A1-, A(2B)-, and A3-AR. The A(2A)-selective sulfostyryl-DMPX derivatives exhibit high water-solubility and may be useful research tools for in vivo studies. Copyright (C) 1998 Elsevier Science Ltd.

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