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107392-33-6

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107392-33-6 Usage

Description

3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE is a chemical compound characterized by the molecular formula C7H6F2N2Cl. It is a salt of benzamidine, known for its role as a reagent in organic synthesis and as an inhibitor in enzymology. 3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE is recognized for its selective inhibitory effects on specific proteases, which positions it as a promising candidate in the development of novel therapeutic agents for a range of diseases. It presents as a white to off-white crystalline powder, and due to its potential irritant properties, it requires careful handling.

Uses

Used in Organic Synthesis:
3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the creation of new compounds and materials.
Used in Enzymology:
In enzymology, 3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE is utilized as an inhibitor, specifically targeting certain proteases. Its selective inhibitory action makes it valuable for studying enzyme functions and for developing drugs that modulate protease activity.
Used in Pharmaceutical Development:
3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE is employed in the development of new drugs due to its potential therapeutic applications. Its capacity to inhibit specific proteases suggests its use in treating diseases where protease activity is a factor, offering a pathway to novel treatment strategies.
Used in Research Applications:
In research settings, 3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE serves as a valuable tool for investigating the mechanisms of action of proteases, their roles in disease processes, and the development of specific inhibitors or activators for these enzymes.
Used in Chemical Compound Libraries:
For the purpose of drug discovery, 3,4-DIFLUORO-BENZAMIDINE HYDROCHLORIDE is included in chemical compound libraries, where it can be screened against biological targets to identify potential leads for medicinal chemistry optimization.

Check Digit Verification of cas no

The CAS Registry Mumber 107392-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,9 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107392-33:
(8*1)+(7*0)+(6*7)+(5*3)+(4*9)+(3*2)+(2*3)+(1*3)=116
116 % 10 = 6
So 107392-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F2N2.ClH/c8-5-2-1-4(7(10)11)3-6(5)9;/h1-3H,(H3,10,11);1H

107392-33-6SDS

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 3,4-Difluorobenzimidamide hydrochloride

1.2 Other means of identification

Product number -
Other names 3,4-Difluoro-benzamidine hydrochloride

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:107392-33-6 SDS

107392-33-6Upstream product

107392-33-6Downstream Products

107392-33-6Relevant articles and documents

Pyrimidine derivatives and liquid crystal compositions including same

-

, (2008/06/13)

2-phenyl-5-(4'-trans-cyclohexyl) phenyl pyrimidine derivatives represented by the general formula: STR1 wherein R is a straight chain alkyl group having 1 to 10 carbon atoms; X is CN or F; Y is F or H; Z is F or H; and when X is F, at least one of Y and Z is H; and the cyclohexane ring is a trans isomer, exhibiting a nematic phase and having a high nematic phase-isotropic liquid phase transition temperature (N-I Point) and large positive dielectric constant anisotropy (Δε). The pyrimidine derivatives may be included in liquid crystal compositions for improved display devices having a wide temperature range, including a high N-I point, a low threshold voltage and a low driving voltage.

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