1162-10-3 Usage
Chemical compound
A substance formed by the chemical combination of two or more elements in a fixed proportion.
Crinan alkaloids
A group of naturally occurring organic compounds that are derived from plants and have various pharmacological properties.
Naturally occurring
Found in nature and not created by humans.
Didehydro group
A chemical group that contains two hydrogen atoms removed from a molecule, which can increase its reactivity and biological activity.
Methoxy groups
Chemical groups that consist of a methyl group (CH3) and an oxygen atom (O), which can be attached to other molecules and influence their properties.
Biological activities
The effects that a compound has on living organisms, such as its ability to inhibit the growth of fungi or bacteria.
Antifungal
A substance that can inhibit the growth of fungi.
Antimicrobial
A substance that can inhibit the growth of microorganisms, such as bacteria.
Pharmacological properties
The effects that a compound has on the body, including its potential to treat or prevent disease.
Medicinal properties
The properties of a compound that make it useful in the treatment or prevention of disease.
Drug development
The process of discovering and developing new drugs and therapeutic agents to treat or prevent disease.
Therapeutic agents
Substances that are used to treat or prevent disease.
Check Digit Verification of cas no
The CAS Registry Mumber 1162-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1162-10:
(6*1)+(5*1)+(4*6)+(3*2)+(2*1)+(1*0)=43
43 % 10 = 3
So 1162-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H21NO4/c1-20-11-3-4-18-5-6-19(15(18)7-11)9-12-13(18)8-14-17(16(12)21-2)23-10-22-14/h3-4,8,11,15H,5-7,9-10H2,1-2H3/t11-,15+,18+/m0/s1
1162-10-3Relevant academic research and scientific papers
Bioinspired enantioselective synthesis of crinine-type alkaloids: Via iridium-catalyzed asymmetric hydrogenation of enones
Zuo, Xiao-Dong,Guo, Shu-Min,Yang, Rui,Xie, Jian-Hua,Zhou, Qi-Lin
, p. 6202 - 6206 (2017/08/29)
A bioinspired enantioselective synthesis of crinine-type alkaloids has been developed by iridium-catalyzed asymmetric hydrogenation of racemic cycloenones. The method features a biomimetic stereodivergent resolution of the substrates bearing a remote arylated quaternary stereocenter. Using this protocol, 24 crinine-type alkaloids and 8 analogues were synthesized in a concise and rapid way with high yield and high enantioselectivity.
