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3-Aminobenzylmethylamine, a chemical compound with the molecular formula C9H13N, is a derivative of benzylamine. It is a clear, colorless to pale yellow liquid with a faint amine odor. Known for its versatility, 3-Aminobenzylmethylamine serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals, playing a significant role in organic synthesis as a building block for a wide range of chemicals.

18759-96-1

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18759-96-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Aminobenzylmethylamine is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of diverse medicinal compounds, enhancing the range of treatments available for various health conditions.
Used in Agrochemical Industry:
3-Aminobenzylmethylamine is utilized as a versatile intermediate in the production of agrochemicals, such as pesticides and herbicides. Its role in the synthesis of these chemicals helps improve agricultural productivity and crop protection, ensuring food security and sustainable farming practices.
Used in Organic Synthesis:
As a building block in organic synthesis, 3-Aminobenzylmethylamine is used for the preparation of a wide range of chemical compounds. Its reactivity and functional groups enable the formation of various organic molecules, which can be further utilized in different industries, including chemical manufacturing, materials science, and research.
It is important to handle 3-Aminobenzylmethylamine with care and take proper safety precautions when working with it in laboratory or industrial settings to ensure the safety of personnel and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 18759-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,5 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18759-96:
(7*1)+(6*8)+(5*7)+(4*5)+(3*9)+(2*9)+(1*6)=161
161 % 10 = 1
So 18759-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-10-6-7-3-2-4-8(9)5-7/h2-5,10H,6,9H2,1H3

18759-96-1SDS

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 3-(methylaminomethyl)aniline

1.2 Other means of identification

Product number -
Other names 3-Amino-N-monomethylbenzylamine

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:18759-96-1 SDS

18759-96-1Downstream Products

18759-96-1Relevant articles and documents

Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts

Cheung, Chi Wai,Surry, David S.,Buchwald, Stephen L.

supporting information, p. 3734 - 3737 (2013/08/23)

A method for the Pd-catalyzed arylation of ammonia with a wide range of aryl and heteroaryl halides, including challenging five-membered heterocyclic substrates, is described. Excellent selectivity for monoarylation of ammonia to primary arylamines was achieved under mild conditions or at rt by the use of bulky biarylphosphine ligands (L6, L7, and L4) as well as their corresponding aminobiphenyl palladacycle precatalysts (3a, 3b, and 3c). As this process requires neither the use of a glovebox nor high pressures of ammonia, it should be widely applicable.

NOVEL CATALYSTS

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Page/Page column 62, (2012/06/01)

The present invention provides novel compounds and ligands that are useful in transition metal catalyzed cross-coupling reactions. For example, the compounds and ligands of the present invention are useful in palladium or gold catalyzed cross-coupling reactions.

A P,N-Ligand for palladium-catalyzed ammonia arylation: Coupling of deactivated aryl chlorides, chemoselective arylations, and room temperature reactions

Lundgren, Rylan J.,Peters, Brendan D.,Alsabeh, Pamela G.,Stradiotto, Mark

supporting information; experimental part, p. 4071 - 4074 (2010/07/05)

(Figure Presented) Amazing ammonia: A new air-stable P,N-ligand (Mor-DalPhos) is reported that enables the palladium-catalyzed crosscoupling of ammonia to a variety of aryl chloride and aryl tosylate substrates with high chemoselectivity and, for the first time, at room temperature (see scheme; Ad = adamantyl, Ts=para-toluenesulfonyl).

Synthesis of potent and selective 2-azepanone inhibitors of human tryptase

Zhao, Guohua,Bolton, Scott A.,Kwon, Chet,Hartl, Karen S.,Seiler, Steven M.,Slusarchyk, William A.,Sutton, James C.,Bisacchi, Gregory S.

, p. 309 - 312 (2007/10/03)

The serine protease tryptase has been associated with a broad range of allergic and inflammatory diseases and, in particular, has been implicated as a critical mediator of asthma. The inhibition of tryptase therefore has the potential to be a valuable therapy for asthma. The synthesis, employing solution phase parallel methods, and SAR of a series of novel 2-azepanone tryptase inhibitors are presented. A member of this series, 8t, was identified as a potent inhibitor of human tryptase (IC50=38 nM) with selectivity ≤330-fold versus related serine proteases (trypsin, plasmin, uPA, tPA, APC, alpha-thrombin, and FXa).

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