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Dithiophen-2-ylphosphinic acid is an organic compound with the chemical formula C6H5PS2. It is a derivative of phosphinic acid, featuring a dithiophene ring (a fused ring system of two thiophene units) attached to the phosphorus atom. dithiophen-2-ylphosphinic acid is of interest in the field of organic chemistry and materials science, particularly for its potential applications in the synthesis of novel materials and as a building block for the development of new pharmaceuticals or organic electronic devices. Its unique structure allows for various chemical modifications and interactions, making it a versatile component in the design of complex molecules and materials.

5849-47-8

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5849-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5849-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5849-47:
(6*5)+(5*8)+(4*4)+(3*9)+(2*4)+(1*7)=128
128 % 10 = 8
So 5849-47-8 is a valid CAS Registry Number.

5849-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dithiophen-2-ylphosphinic acid

1.2 Other means of identification

Product number -
Other names Phosphinic acid,di-2-thienyl

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:5849-47-8 SDS

5849-47-8Relevant academic research and scientific papers

Bis-2-thienyldiethylaminophosphane as a ligand in late transition metal complexes and its transformation to bis-2-thienylphosphane

Granitzka, Markus,Stollberg, Peter,Stalke, Dietmar

supporting information, p. 1429 - 1440 (2015/06/16)

Bis-2-thienyldiethylaminophosphane (C4H3S)2PNEt2 (1) is introduced as a ligand for late transition metal complexes ([(H3C4S)2PNEt2]nMXmLp/s

Rhodium-catalyzed oxidative C-H activation/cyclization for the synthesis of phosphaisocoumarins and phosphorous 2-pyrones

Park, Youngchul,Seo, Jungmin,Park, Sangjune,Yoo, Eun Jeong,Lee, Phil Ho

supporting information, p. 16461 - 16468 (2013/12/04)

Rhodium-catalyzed cyclization of phosphinic acids and phosphonic monoesters with alkynes has been developed. The oxidative annulation proceeds with complete conversion of phosphinic acid derivatives and allowed the atom-economic preparation of useful phosphaisocoumarins with high yield and selectivity. The reaction is tolerant of extensive substitution on the phosphinic acid, phosphonic monoester and alkyne, including halides, ketone, and hydroxyl groups as substituents. Furthermore, we found that alkenylphosphonic monoesters proceed to give a wide range of phosphorus 2-pyrones through oxidative annulation with alkynes. Mechanistic studies revealed that Ci£H bond metalation was the rate-limiting step. Copyright

Synthesis and structural studies (1H, 13C, 31P NMR and X-ray) of new C-bonded cyclotriphosphazenes with heterocyclic substituents from novel phosphinic acid derivatives

Vicente, Virginie,Fruchier, Alain,Taillefer, Marc,Combes-Chamalet, Corinne,Scowen, Ian J.,Plenat, Francoise,Cristau, Henri-Jean

, p. 418 - 424 (2007/10/03)

Three new C-bonded cyclotriphosphazenes, [N3P 3(2-thienyl)6], 2, [N3P3(3-thienyl) 6], 4, and [N3P3(3,3′-bithienyl-2, 2′-ylene)3], 6, have been prepared by two new synthetic procedures and are the first examples of non-spiro and trispirocyclotriphosphazene derivatives composed of thiophene and 3,3′-dithiophene substituents, respectively. Their 1H, 13C and 31P NMR parameters are given. The solid state structures of 2, 4 and 6 have been determined by X-ray crystallography.

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