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Benzene, 1-chloro-4-(propylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101167-08-2

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101167-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101167-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,1,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101167-08:
(8*1)+(7*0)+(6*1)+(5*1)+(4*6)+(3*7)+(2*0)+(1*8)=72
72 % 10 = 2
So 101167-08-2 is a valid CAS Registry Number.

101167-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-propylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names 1-chloro-4-(propylsulfonyl)benzene

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:101167-08-2 SDS

101167-08-2Downstream Products

101167-08-2Relevant academic research and scientific papers

Nickel(II)-Catalyzed Synthesis of Sulfinates from Aryl and Heteroaryl Boronic Acids and the Sulfur Dioxide Surrogate DABSO

Lo, Pui Kin Tony,Chen, Yiding,Willis, Michael C.

, p. 10668 - 10673 (2019/11/11)

We report a redox-neutral Ni(II)-catalyzed sulfination of readily available aryl and heteroaryl boronic acids. Using the combination of commercially available, air-stable NiBr2·(glyme), a commercially available phenanthroline ligand, and DABSO, boronic acids are efficiently converted to the corresponding sulfinate salts, which can be further elaborated to valuable sulfonyl-containing groups, including sulfones, sulfonamides, sulfonyl fluorides, and sulfonate esters. The catalyst loading can be reduced to 2.5 mol ?% on a gram scale. This practically simple protocol tolerates an unprecedented range of pharmaceutically relevant and electron-poor (hetero)aryl boronic acids, allowing the direct synthesis of active pharmaceutical ingredients.

Palladium-Catalyzed Synthesis of (Hetero)Aryl Alkyl Sulfones from (Hetero)Aryl Boronic Acids, Unactivated Alkyl Halides, and Potassium Metabisulfite

Shavnya, Andre,Hesp, Kevin D.,Mascitti, Vincent,Smith, Aaron C.

supporting information, p. 13571 - 13575 (2015/11/16)

A palladium-catalyzed one-step synthesis of (hetero)aryl alkyl sulfones from (hetero)arylboronic acids, potassium metabisulfite, and unactivated or activated alkylhalides is described. This transformation is of broad scope, occurs under mild conditions, and employs readily available reactants. A stoichiometric experiment has led to the isolation of a catalytically active dimeric palladium sulfinate complex, which was characterized by X-ray diffraction analysis.

PHENOXY ACETIC ACID DERIVATIVES

-

Page/Page column 114-115, (2010/09/03)

The present invention provides phenoxyacetic acid derivatives of Formula (I) for the treatment of CRTH2 related disorders and disease selected from asthma, atopic dermatitis and inflammatory dermatoses.

ELECTRONIC EFFECTS IN ALKYL 4-CHLOROPHENYL SULFONE AND SULFOXIDE MOLECULES ACCORDING TO 35Cl NQR DATA

Feshin, V. P.,Voronkov, M. G.,Dolgushin, G. V.,Romanenko, L. S.,Aliev, I. A.,Mirzoeva, M. A.

, p. 1103 - 1106 (2007/10/02)

Compounds of the 4-ClC6H4S(O)CHn.(CH3)3-n and 4-ClC6H4SO2R series nH and CHn(CH3)3-n> were synthesized and studied by the 35Cl NQR method.It was found that their NQR frequencies change regularly with increase in the number n.

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