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2-Methylpropionamidine, with the chemical formula C4H10N2, is a colorless liquid derivative of propionamide. It possesses a pungent odor and is highly soluble in water. 2-METHYLPROPIONAMIDINE is utilized in various applications, including organic synthesis as a reagent and as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it serves as a catalyst in certain chemical reactions. Due to its potential harmful effects, it is crucial to handle 2-Methylpropionamidine with care to avoid skin, eye contact, ingestion, or inhalation.

57536-10-4

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57536-10-4 Usage

Uses

Used in Organic Synthesis:
2-Methylpropionamidine is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of desired products in the synthesis of complex organic compounds.
Used in Pharmaceutical Production:
As an intermediate, 2-Methylpropionamidine plays a crucial role in the production of pharmaceuticals. Its involvement in the synthesis process aids in the creation of active pharmaceutical ingredients, which are vital for developing effective medications.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, 2-Methylpropionamidine is utilized as an intermediate in the synthesis of various agrochemicals. This contributes to the development of products that help protect crops and enhance agricultural productivity.
Used as a Catalyst in Chemical Reactions:
2-Methylpropionamidine is also employed as a catalyst to accelerate specific chemical reactions. Its catalytic properties enable more efficient and faster reaction rates, which is beneficial in various industrial processes.
Safety Precautions:
Given the potential hazards associated with 2-Methylpropionamidine, it is essential to handle this chemical with appropriate safety measures. This includes wearing protective gear, such as gloves and goggles, to prevent skin and eye contact. Additionally, ensuring proper ventilation and following safe handling procedures can minimize the risk of ingestion or inhalation.

Check Digit Verification of cas no

The CAS Registry Mumber 57536-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57536-10:
(7*5)+(6*7)+(5*5)+(4*3)+(3*6)+(2*1)+(1*0)=134
134 % 10 = 4
So 57536-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2/c1-3(2)4(5)6/h3H,1-2H3,(H3,5,6)

57536-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYLPROPIONAMIDINE

1.2 Other means of identification

Product number -
Other names PropaniMidaMide,2-Methyl

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:57536-10-4 SDS

57536-10-4Relevant academic research and scientific papers

DIPEPTIDYL PEPTIDASE-IV INHIBITING COMPOUNDS, METHODS OF PREPARING THE SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AS AN ACTIVE AGENT

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Page/Page column 134-135, (2010/11/24)

The present invention relates to novel compounds exhibiting good inhibitory activity versus Dipeptidyl Peptidase-IV(DPP-IV), methods of preparing the same and pharmaceutical compositions containing the same as an active agent.

Inhibitors of human nitric oxide synthase isoforms with the carbamidine moiety as a common structural element

Moore, William M.,Webber, R. Keith,Fok, Kam F.,Jerome, Gina M.,Kornmeier, Christine M.,Tjoeng, Foe S.,Currie, Mark G.

, p. 1559 - 1564 (2007/10/03)

Identification of potent and selective inhibitors of inducible nitric oxide synthase (NOS) is of great interest because of their therapeutic potential for treatment of diseases mediated by excess production of nitric oxide. We present here a comparison of

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