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α,α-Bis-(3,3-dimethylallyl)phenylacetonitril, also known as 1,1'-(1,2-phenylene)bis[3,3-dimethyl-2-cyano-2-propen-1-yl], is a synthetic organic compound characterized by its molecular formula C19H23N. It is a derivative of phenylacetonitril, featuring two 3,3-dimethylallyl groups attached to the phenyl ring. α,α-Bis-(3,3-dimethylallyl)phenylacetonitril is known for its potential applications in the synthesis of various organic compounds and may be used as an intermediate in the production of pharmaceuticals, agrochemicals, or other specialty chemicals. Its structure, with the phenyl ring and the cyano group, suggests that it could be involved in reactions that lead to the formation of complex molecules. However, specific applications and properties would depend on the context in which it is used, and further research or information would be needed to detail its specific uses and characteristics.

38179-53-2

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38179-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38179-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38179-53:
(7*3)+(6*8)+(5*1)+(4*7)+(3*9)+(2*5)+(1*3)=142
142 % 10 = 2
So 38179-53-2 is a valid CAS Registry Number.

38179-53-2Downstream Products

38179-53-2Relevant academic research and scientific papers

Chiral Sulfide Catalysis for Desymmetrizing Enantioselective Chlorination

Cao, Qingxiang,Luo, Jie,Zhao, Xiaodan

, p. 1315 - 1319 (2019)

An unprecendented chiral sulfide catalyzed desymmetrizing enantioselective chlorination is disclosed. Various aryl-tethered diolefins and diaryl-tethered olefins afforded teralins and tricyclic hexahydrophenalene derivatives, respectively, bearing multiple stereogenic centers in high yields with excellent enantio- and diastereoselectivities. In contrast, the tertiary amine catalyst (DHQD)2PHAL led to a diastereomeric product. The products could be transformed into a variety of compounds, such as spiro-N-heterocycles.

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