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50466-15-4

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50466-15-4 Usage

General Description

4-Methoxycarbonylbenzamidine dihydrochloride is a chemical compound used in research laboratories and pharmaceutical development. It is a potent and selective inhibitor of blood coagulation factor Xa, making it a valuable tool in the study of blood clotting and related disorders. 4-METHOXYCARBONYLBENZAMIDINE DIHYDROCHLORIDE is also being investigated for its potential therapeutic applications in the treatment of thrombotic diseases. Additionally, 4-Methoxycarbonylbenzamidine dihydrochloride may have utility in the development of new anticoagulant medications with improved safety and efficacy profiles. Overall, this compound plays a crucial role in advancing our understanding of blood coagulation and may hold promise for the future treatment of coagulation disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 50466-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,6 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50466-15:
(7*5)+(6*0)+(5*4)+(4*6)+(3*6)+(2*1)+(1*5)=104
104 % 10 = 4
So 50466-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O2/c1-13-9(12)7-4-2-6(3-5-7)8(10)11/h2-5H,1H3,(H3,10,11)

50466-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxycarbonyl-benzamidine

1.2 Other means of identification

Product number -
Other names 4-METHOXYCARBONYLBENZAMIDINE DIHYDROCHLORIDE

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:50466-15-4 SDS

50466-15-4Relevant articles and documents

Preparation of amidines by amidoxime reduction with potassium formate

Nadrah, Kristina,Dolenc, Marija Sollner

, p. 1257 - 1258 (2008/02/08)

Amidines can be prepared by reducing acylated amidoxime with potassium formate. The method has proved to be very simple and effective. Georg Thieme Verlag Stuttgart.

Synthesis of esters of guanidinobenzoic acids and guanidinomethylbenzoic acids with antiproteolytic activity

Wagner,Vieweg,Kuehmstedt

, p. 293 - 296 (2007/10/06)

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