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51335-90-1

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51335-90-1 Usage

General Description

1-[5-(4-CHLOROPHENYL)-2-THIENYL]-1-ETHANONE is a chemical compound with the molecular formula C12H9ClOS. It is a ketone that contains a thiophene ring with a chlorophenyl group attached to it. 1-[5-(4-CHLOROPHENYL)-2-THIENYL]-1-ETHANONE is commonly used in the synthesis of pharmaceuticals as well as in the production of various organic compounds. It is important to handle this chemical with care as it may pose a risk to health and safety if not properly managed. Additionally, it is also essential to follow proper storage and disposal protocols for this compound to prevent any potential hazards to the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 51335-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,3 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51335-90:
(7*5)+(6*1)+(5*3)+(4*3)+(3*5)+(2*9)+(1*0)=101
101 % 10 = 1
So 51335-90-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H9ClOS/c1-8(14)11-6-7-12(15-11)9-2-4-10(13)5-3-9/h2-7H,1H3

51335-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[5-(4-Chlorophenyl)-2-thienyl]-1-ethanone

1.2 Other means of identification

Product number -
Other names 1-[5-(4-chlorophenyl)thiophen-2-yl]ethanone

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:51335-90-1 SDS

51335-90-1Relevant articles and documents

A Zwitterionic Palladium(II) Complex as a Precatalyst for Neat-Water-Mediated Cross-Coupling Reactions of Heteroaryl, Benzyl, and Aryl Acid Chlorides with Organoboron Reagents

Ramakrishna, Visannagari,Rani, Morla Jhansi,Reddy, Nareddula Dastagiri

, p. 7238 - 7255 (2018/01/01)

The Suzuki–Miyaura cross-coupling (SMC) reactions of several heteroaryl chlorides, benzyl chlorides, and aryl acid chlorides with (hetero)arylboron reagents have been investigated in the presence of [Pd(HL1)(PPh3)Cl2] (I) [HL1 = 3-[(2,6-diisopropylphenyl)-1-imidazolio]-2-quinoxalinide] as catalyst and K2CO3 as base in neat water. The synthesis of the heterocycle-containing biaryls required the addition of 2 mol-% of a phosphine ligand (PPh3 or X-Phos). A combination of more than 115 substrates were screened and it was found that I is a versatile catalyst that can produce heterocycle-containing biaryls, diarylmethanes, and benzophenones in moderate-to-excellent yields.

Phenyl-thienyl-alkanoic acid derivatives and phenyl-furyl-alkanoic acid derivatives

-

, (2008/06/13)

Phenyl-thienyl-alkanoic acid derivatives and phenyl-furyl-alkanoic acid derivatives, processes for their preparation, and pharmaceutical compositions comprising them. Compounds have anti-inflammatory, hypocholesterolaemic, analgesic and antipyretic activi

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