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4-Cyano-4-methyl-4-phenyl-butyric acid is a synthetic organic compound characterized by its molecular formula C13H13NO2. It features a butyric acid backbone with a cyano group (-CN), a methyl group (-CH3), and a phenyl group (C6H5) attached to the fourth carbon atom. 4-Cyano-4-methyl-4-phenyl-butyric acid is known for its potential applications in the synthesis of pharmaceuticals and other chemical products due to its unique structural properties. It is typically used as an intermediate in the production of various drugs and is also found in research settings for the development of new chemical entities. The compound's specific structure allows it to participate in a range of chemical reactions, making it a valuable component in the field of organic chemistry.

1135-74-6

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1135-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1135-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1135-74:
(6*1)+(5*1)+(4*3)+(3*5)+(2*7)+(1*4)=56
56 % 10 = 6
So 1135-74-6 is a valid CAS Registry Number.

1135-74-6Relevant academic research and scientific papers

Relative Migratory Aptitudes of Doubly and Triply Bonded Groups in a Cycloheptatriene System

Battye, Peter J.,Jones, David W.

, p. 1479 - 1490 (2007/10/02)

In cyclopentadiene systems, 1,5-shift of triply bonded groups is much slower than that of doubly bonded groups, whereas in the cycloheptatriene systems (34) and (29), as well as in (21) and (19), CN and CHO groups have very similar migratory tendencies.In

2,6-Piperidinediones, I: Synthesis of the Racemates and Enantiomers of 3,3-Disubstituted 2,6-Piperidinediones

Knabe, Joachim,Reischig, Dirk

, p. 353 - 362 (2007/10/02)

The synthesis of the racemates and the enantiomers of the 3,3-disubstituted 2,6-piperidinediones 3a-3g is performed in three ways, depending on the C-3 substituents.The 3-cyclohexylpiperidinedione 3h is obtained as racemic and optically active compound by

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