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4-Bromo-2,6-dichlorobenzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99835-27-5

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99835-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99835-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,3 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99835-27:
(7*9)+(6*9)+(5*8)+(4*3)+(3*5)+(2*2)+(1*7)=195
195 % 10 = 5
So 99835-27-5 is a valid CAS Registry Number.
InChI:InChI=1S/C7H2BrCl2N/c8-4-1-6(9)5(3-11)7(10)2-4/h1-2H

99835-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-2,6-dichlorobenzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,4-bromo-2,6-dichloro

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:99835-27-5 SDS

99835-27-5Downstream Products

99835-27-5Relevant academic research and scientific papers

TYK2 INHIBITORS AND USES THEREOF

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Paragraph 00315; 00316, (2015/09/28)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Palladium-catalyzed highly selective ortho-halogenation (I, Br, Cl) of arylnitriles via sp2 C-H bond activation using cyano as directing group

Du, Bingnan,Jiang, Xiaoqing,Sun, Peipei

, p. 2786 - 2791 (2013/04/24)

A palladium-catalyzed ortho-halogenation (I, Br, Cl) of arylnitrile is described. The optimal reaction conditions were identified after examining various factors such as catalyst, additive, solvent, and reaction temperature. Using cyano as the directing group, the halogenation reaction gave good to excellent yields. The method is compatible to the arylnitriles with either electron-withdrawing or electron-donating groups. The reaction is available to the substrate in at least gram scale. The present method was successfully applied to the synthesis of the precursors of paucifloral F and isopaucifloral F.

INDOLE SULFONAMIDE MODULATORS OF PROGESTERONE RECEPTORS

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Page/Page column 27, (2008/06/13)

Compounds of Formula (I), wherein n is 1 or 2, and R1, R2, R3, R4, R5, R6, R7, and R8 are as defined herein, their preparation, pharmaceutical compositions, and methods of use are disclosed.

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