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3-MethylpicoliniMidaMide hydrochloride is a versatile chemical compound utilized in the field of organic chemistry, serving as a crucial intermediate in the synthesis of a variety of organic compounds. It is renowned for its adaptable chemical properties and is frequently employed as a reagent in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it functions as a building block in the preparation of complex molecules and acts as a catalyst in numerous chemical reactions, making it an indispensable tool in synthetic chemistry.
Used in Pharmaceutical Industry:
3-MethylpicoliniMidaMide hydrochloride is used as a reagent for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing ones.
Used in Agrochemical Industry:
3-MethylpicoliniMidaMide hydrochloride is used as a reagent in the production of agrochemicals, aiding in the creation of innovative products to enhance crop protection and yield.
Used in Organic Synthesis:
3-MethylpicoliniMidaMide hydrochloride is used as a building block for the preparation of complex molecules, facilitating the construction of intricate chemical structures for a wide range of applications.
Used as a Catalyst in Chemical Reactions:
3-MethylpicoliniMidaMide hydrochloride is used as a catalyst to accelerate various chemical reactions, enhancing the efficiency and selectivity of synthetic processes in organic chemistry.

125903-77-7

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125903-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125903-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,0 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125903-77:
(8*1)+(7*2)+(6*5)+(5*9)+(4*0)+(3*3)+(2*7)+(1*7)=127
127 % 10 = 7
So 125903-77-7 is a valid CAS Registry Number.

125903-77-7SDS

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-methylpyridine-2-carboximidamide,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-methylpicolinimidamide 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:125903-77-7 SDS

125903-77-7Upstream product

125903-77-7Downstream Products

125903-77-7Relevant academic research and scientific papers

NOVEL TETRAHYDROPYRIDOPYRIMIDINES AND TETRAHYDROPYRIDOPYRIDINES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

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Page/Page column 37, (2016/07/27)

The invention provides novel compounds having the general formula (I): wherein R1, R2, R3, Q, U,W, Z, X and Y are as described herein, compositions including the compounds and methods of using the compounds. These compounds are HbsAg inhibitors and are useful as medicaments for the treatment or prophylaxis of HBV infection.

2, 6 BISHETEROARYL-4-AMINOPYRIMIDINES AS ADENOSINE RECEPTOR ANTAGONISTS

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Page/Page column 96, (2010/02/12)

4-Aminopyrimidine derivatives of formula (I) FORMULA heteroaryl groups, including pharmaceutically acceptable salts thereof, wherein R1 and R2 are adenosine A2A receptor antagonists useful in the treatment of movement disorders such as Parkinson's disease.

Preparation of Triazolopyrimidines as Potential Antiasthma Agents

Medwid, Jeffrey B.,Paul, Rolf,Baker, Jannie S.,Brockman, John A.,Du, Mila T.,et al.

, p. 1230 - 1241 (2007/10/02)

With the use of the human basophil histamine release assay, 5-aryl-2-aminotriazolopyrimidines were found to be active as mediator release inhibitors.These compounds were prepared by reacting arylamidines with sodium ethyl formylacetate or with ethyl propiolate to give pyrimidinones.Treatment with phosphorus oxychloride gave a chloropyrimidine, which was converted to a hydrazinopyrimidine with hydrazine.Cyclization, using cyanogen bromide, gave the triazolopyrimidines, after a Dimroth rearrangement.Following a structure-activity evaluation, the5--2-amino (8-10), 5-(3-bromophenyl)-2-amino (8-13), 5--2-amino (8-11), and 5-(4-pyridinyl)-2-amino (6-7) compounds were found to have the best activity.They were chosen for further pharmacological and toxicological study.

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