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(4-isopropyl-benzylidene)-((R)-1-phenyl-ethyl)-amine is a complex organic compound with the molecular formula C22H23N. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the "R" in its name indicates that it is the right-handed enantiomer. (4-isopropyl-benzylidene)-((R)-1-phenyl-ethyl)-amine features a benzylidene group (a carbon-carbon double bond between a benzene ring and a carbon atom) connected to an isopropyl group (a propyl group with a methyl group attached to the second carbon). Additionally, it has a phenylethylamine group, which consists of a phenyl ring attached to an ethylamine chain. This chemical structure is significant in the field of pharmaceuticals and chemistry, as it may exhibit specific biological activities or be used as an intermediate in the synthesis of other compounds.

4187-49-9

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4187-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4187-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,8 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4187-49:
(6*4)+(5*1)+(4*8)+(3*7)+(2*4)+(1*9)=99
99 % 10 = 9
So 4187-49-9 is a valid CAS Registry Number.

4187-49-9Downstream Products

4187-49-9Relevant academic research and scientific papers

Asymmetric induction in the addition of enantiomerically pure H-phosphinate to chiral aldimines: diastereoselective generation of α-amino phosphinates with P,C-stereogenic centers

Yang, Meng,Xu, Hao,Zhou, Zhong-Yang,Zhang, He,Liu, Li-Juan,Sun, Yong-Ming,Nie, Shao-Zhen,Zhao, Chang-Qiu

, p. 815 - 822 (2016)

α-Amino phosphinates with P,C-stereogenic centers were prepared from a P-retained addition of (RP)-(?)-menthyl H-phenylphosphinate to (R)-aldimines with up to 86:14 dr under catalyst and solvent free condition at ambient temperature; the single

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