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(1R)-1-(4-chlorophenyl)propan-1-amine hydrochloride is a chemical compound belonging to the class of organic compounds known as aralkylamines. It is commonly used as a precursor in the synthesis of other important organic compounds and has potential applications in medicinal chemistry, particularly in the development of new pharmaceutical drugs. Its hydrochloride form is the salt form of the compound, often used for pharmaceutical purposes, and it has the potential to exhibit various biological activities due to its structural properties.

1448902-18-8

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1448902-18-8 Usage

Uses

Used in Pharmaceutical Industry:
(1R)-1-(4-chlorophenyl)propan-1-amine hydrochloride is used as a precursor in the synthesis of other important organic compounds for the development of new pharmaceutical drugs. Its structural properties allow it to exhibit various biological activities, making it a valuable compound for scientific research and application in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1448902-18-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,9,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1448902-18:
(9*1)+(8*4)+(7*4)+(6*8)+(5*9)+(4*0)+(3*2)+(2*1)+(1*8)=178
178 % 10 = 8
So 1448902-18-8 is a valid CAS Registry Number.

1448902-18-8Relevant academic research and scientific papers

Synthesis and optimization of novel (3S,5R)-5-(2,2-dimethyl-5-oxo-4- phenylpiperazin-1-yl)piperidine-3-carboxamides as orally active renin inhibitors

Mori, Yutaka,Ogawa, Yasuyuki,Mochizuki, Akiyoshi,Nakamura, Yuji,Fujimoto, Teppei,Sugita, Chie,Miyazaki, Shojiro,Tamaki, Kazuhiko,Nagayama, Takahiro,Nagai, Yoko,Inoue, Shin-Ichi,Chiba, Katsuyoshi,Nishi, Takahide

, p. 5907 - 5922 (2013/09/12)

We report synthesis and optimization of a series of (3S,5R)-5-(2,2- dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as renin inhibitors. Chemical modification of P1, P2 and P 3 portions led to a promising 3

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