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1033225-44-3

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1033225-44-3 Usage

General Description

1-N-(2,6-difluorophenyl)benzene-1,2-diamine is an organic compound with the chemical formula C12H11F2N. It is a type of benzene-1,2-diamine, which is a class of compounds containing two amine groups attached to a benzene ring. The 2,6-difluorophenyl substitution indicates that two fluorine atoms are attached to the phenyl group at the 2 and 6 positions. This chemical is primarily used as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. It possesses potential applications in the fields of medicinal chemistry and material science due to its diverse reactivity and structure.

Check Digit Verification of cas no

The CAS Registry Mumber 1033225-44-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,2,2 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1033225-44:
(9*1)+(8*0)+(7*3)+(6*3)+(5*2)+(4*2)+(3*5)+(2*4)+(1*4)=93
93 % 10 = 3
So 1033225-44-3 is a valid CAS Registry Number.

1033225-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N-(2,6-difluorophenyl)benzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names N1-(2,6-difluorophenyl)benzene-1,2-diamine

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:1033225-44-3 SDS

1033225-44-3Relevant articles and documents

Development of a pilot-plant-scale synthesis of an alkylated dihydrobenzothiadiazole S, S-dioxide: Incorporation of a late-stage mitsunobu reaction

Connolly, Terrence J.,Auguscinski, Waldemar,Fung, Peter,Galante, Rocco,Liu, Weiguo,McGovern, Linda,Sebastian, Alice,Shen, Xiaole,Shi, Xinxu,Wilk, Boguslawa,Varsalona, Richard,Zhong, Huijuan

, p. 868 - 877 (2011/03/20)

The process used to prepare a functionalized dihydrobenzothiadiazole S,S-dioxide on a pilot plant scale is described. Key changes to the original synthesis included: modifying SNAr reaction conditions between a substituted aniline and 2-fluoron

ARYL SULFAMIDE DERIVATIVES AND METHODS OF THEIR USE

-

Page/Page column 136, (2008/12/06)

The present invention is directed to aryl sulfamide derivatives of formula (I): or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof, which are monoamine reuptake inhibitors, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions, including, inter alia, vasomotor symptoms, sexual dysfunction, gastrointestinal disorders and genitourinary disorder, depression disorders, endogenous behavioral disorders, cognitive disorders, diabetic neuropathy, pain, and other diseases or disorders.

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