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2-(methyl(phenethyl)amino)acetonitrile is a chemical compound with the molecular formula C11H14N2. It is an organic compound that features a phenethylamine structure, which is a derivative of amphetamine. 2-(methyl(phenethyl)amino)acetonitrile is characterized by a phenethyl group (a benzene ring attached to an ethyl group) connected to a methyl group, which in turn is bonded to a 2-aminoacetonitrile moiety. The presence of the nitrile group (-CN) gives it unique chemical properties. 2-(methyl(phenethyl)amino)acetonitrile is of interest in the field of medicinal chemistry and may have potential applications in the development of pharmaceuticals due to its structural similarity to certain psychoactive substances. However, it is important to note that the specific uses, safety, and legal status of 2-(methyl(phenethyl)amino)acetonitrile can vary, and it is not approved for medical use. The compound's structure and potential effects should be further investigated within the appropriate scientific and legal frameworks.

1629-35-2

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1629-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1629-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1629-35:
(6*1)+(5*6)+(4*2)+(3*9)+(2*3)+(1*5)=82
82 % 10 = 2
So 1629-35-2 is a valid CAS Registry Number.

1629-35-2Downstream Products

1629-35-2Relevant academic research and scientific papers

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

, p. 18333 - 18337 (2015)

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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