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N-(2,6-dimethyl-phenyl)-β-alanine nitrile is an organic compound with the chemical formula C11H14N2O. It is a derivative of β-alanine, an amino acid, where the phenyl group is substituted with two methyl groups at the 2 and 6 positions, and the amino group is replaced by a nitrile group. N-(2,6-dimethyl-phenyl)-β-alanine nitrile is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as a building block for the creation of more molecules complex. It is also recognized for its role in the development of new materials with unique properties. The compound's structure and reactivity make it a valuable intermediate in organic synthesis, contributing to the advancement of various chemical and biological fields.

6437-71-4

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6437-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6437-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6437-71:
(6*6)+(5*4)+(4*3)+(3*7)+(2*7)+(1*1)=104
104 % 10 = 4
So 6437-71-4 is a valid CAS Registry Number.

6437-71-4Downstream Products

6437-71-4Relevant academic research and scientific papers

Assessment and use of two silicon carbide multi-well plates for library synthesis and proteolytic digests using microwave heating

Stencel, Lauren M.,Kormos, Chad M.,Avery, Keri B.,Leadbeater, Nicholas E.

experimental part, p. 2452 - 2457 (2009/09/26)

The use of two silicon carbide plates is reported for the preparation of three libraries of organic molecules using microwave heating. In addition, a preliminary study has been carried out, showing that one of the plates can also be used in a proteomics setting. Both the 24-position and 48-position plates heated evenly when irradiated with microwave energy. The 48-position plate was used to prepare a library of N-aryl functionalized β-amino esters via an aza-Michael reaction between anilines and Michael acceptors. The 24-position plate was used to prepare a library of biaryls via a Suzuki coupling methodology and a library of 1,4-dihydropyridines via a Hantzsch synthesis. The 48-position plate was also used to perform the proteolytic digestion of insulin chain B by trypsin. The Royal Society of Chemistry 2009.

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