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Chonemorphine is a naturally occurring opioid alkaloid found in the plant Chonemorpha fragrans, which is native to Southeast Asia. It is structurally similar to morphine and has been studied for its potential analgesic properties. Chonemorphine is known to interact with the mu-opioid receptors in the brain, which are responsible for the perception of pain and the experience of pleasure. Due to its opioid nature, it carries the risk of addiction and side effects similar to other opioids, such as respiratory depression, constipation, and dependence. The compound is of interest to researchers for its potential therapeutic applications, but it is not currently used clinically due to the availability of safer and more effective pain management options.

4282-07-9

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4282-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4282-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4282-07:
(6*4)+(5*2)+(4*8)+(3*2)+(2*0)+(1*7)=79
79 % 10 = 9
So 4282-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H42N2/c1-15(25(4)5)19-8-9-20-18-7-6-16-14-17(24)10-12-22(16,2)21(18)11-13-23(19,20)3/h15-21H,6-14,24H2,1-5H3/t15-,16-,17-,18-,19+,20-,21-,22-,23+/m0/s1

4282-07-9Relevant academic research and scientific papers

TRANSFORMATIONS OF SOLASODINE

Khodzhaev, B. U.,Shakirov, R.,Yunusov, S. Yu.

, p. 278 - 281 (2007/10/02)

Solasodine (I) has been subjected to a number of transformations.The following compounds have been obtained from it by described procedures: 3β-acetoxypregna-5,16-dien-20-one (II), 3β-acetoxypregn-5-en-20α-ol (III), and 3β-acetoxypregn-5-en-20β-ol (IV).The oxidation of (III) and (IV), the formation of an oxime, and the reduction of the oxime with sodium in ethanol, followed by Hess methylation, has led to 20α-dimethylaminopregn-5-en-3β-ol (IX) and to 20β-dimethylaminopregn-5-en-3β-ol (X).From compounds (IX) and (X), by analogy with (III) and (IV) by their oxidation and the preparation of oximes, which were then reduced and methylated, the following were obtained: 3β,20α-bisdimethylaminopregnane (XVII) and 3β,20β-bisdimethylaminopregnane (XVIII), and also quaternary salts of the latter.

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