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[ethyl(3-methylphenyl)amino]acetonitrile, also known as 3-methylphenethylamine, is a chemical compound characterized by its molecular formula C11H14N2. It presents as a colorless to pale yellow liquid with a slightly amine-like odor. [ethyl(3-methylphenyl)amino]acetonitrile is recognized for its unique structure and properties, making it a valuable asset in the field of organic chemistry and pharmaceutical research.

63133-74-4

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63133-74-4 Usage

Uses

Used in Pharmaceutical Synthesis:
[ethyl(3-methylphenyl)amino]acetonitrile is utilized as an intermediate in the synthesis of various pharmaceutical drugs. Its distinctive structure allows for the creation of a wide range of medicinal compounds, contributing to the development of novel treatments and therapies.
Used in Organic Chemistry:
[ethyl(3-methylphenyl)amino]acetonitrile also serves as a building block in organic chemistry reactions. Its properties facilitate the formation of new organic compounds, which can be applied across different industries, from pharmaceuticals to materials science.
Used in Chemical Research:
The unique structure and properties of [ethyl(3-methylphenyl)amino]acetonitrile make it an essential tool for researchers and chemists. It aids in the development of new materials and chemical processes, furthering scientific understanding and innovation in the field.
Used in Chemical Process Development:
In the chemical industry, [ethyl(3-methylphenyl)amino]acetonitrile is employed to develop new processes and improve existing ones. Its versatility and reactivity contribute to the advancement of chemical engineering and the creation of more efficient and sustainable methods.

Check Digit Verification of cas no

The CAS Registry Mumber 63133-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63133-74:
(7*6)+(6*3)+(5*1)+(4*3)+(3*3)+(2*7)+(1*4)=104
104 % 10 = 4
So 63133-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2/c1-3-13(8-7-12)11-6-4-5-10(2)9-11/h4-6,9H,3,8H2,1-2H3

63133-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-m-tolyl-glycine nitrile

1.2 Other means of identification

Product number -
Other names N-Aethyl-N-m-tolyl-glycin-nitril

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:63133-74-4 SDS

63133-74-4Downstream Products

63133-74-4Relevant academic research and scientific papers

Preparation method for alpha-cyanoamine

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Paragraph 0068; 0069, (2016/10/07)

The invention discloses a preparation method for alpha-cyanoamine. According to the method, the product alpha-cyanoamine is prepared through nucleophilic substitution in a mixed solvent in the presence of an oxidizing agent with an amine compound and cyanoacetic acid as reactants, iodide as a catalyst and sodium acetate as alkali. The catalyst used in the method has high reactivity; reaction conditions are mild; the application scope of a substrate is wide; post-treatment is convenient; the yield of the target product is high; preparation process is simple, green and environment-friendly; and used raw materials are widely available.

Cyanoacetic Acid as a Masked Electrophile: Transition-Metal-Free Cyanomethylation of Amines and Carboxylic Acids

Wang, Hongxiang,Shao, Ying,Zheng, Hao,Wang, Hanghang,Cheng, Jiang,Wan, Xiaobing

supporting information, p. 18333 - 18337 (2015/12/24)

Using cyanoacetic acid as a masked electrophile, a new cyanomethylation reaction of amines and carboxylic acids was developed, producing a variety of α-aminonitriles and cyanomethyl esters with good yields and excellent functionality tolerance. This protocol features simple manipulation, inexpensive reagents, and a wide substrate scope. Iodoacetonitrile was generated in situ from the iodination-decarboxylation of cyanoacetic acid in this transformation.

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