Baptifoline is a naturally occurring alkaloid compound that belongs to the family of indole alkaloids. It is primarily found in the plant species, such as the African shrub, Tabernaemontana catharinensis, and has been reported to possess various pharmacological properties. The compound has been studied for its potential anti-inflammatory, anti-cancer, and anti-malarial effects, making it a subject of interest in the field of medicinal chemistry. However, further research is needed to fully understand its therapeutic potential and safety profile.

732-50-3

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Basic information
1. Product Name: baptifoline
2. Synonyms: baptifoline;(7R)-7,7aα,8,9,10,11,13,14-Octahydro-9β-hydroxy-7β,14β-methano-4H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocin-4-one
3. CAS NO:732-50-3
4. Molecular Formula: C15H20N2O2
5. Molecular Weight: 260.33
6. EINECS: N/A
7. Product Categories: N/A
Chemical Properties
1. Melting Point: N/A
2. Boiling Point: 528.2°C at 760 mmHg
3. Flash Point: 273.2°C
4. Appearance: /
5. Density: 1.31g/cm³
6. Vapor Pressure: 2.32E-13mmHg at 25°C
7. Refractive Index: 1.653
8. Storage Temp.: N/A
9. Solubility: N/A
10. CAS DataBase Reference: baptifoline(CAS DataBase Reference)
11. NIST Chemistry Reference: baptifoline(732-50-3)
12. EPA Substance Registry System: baptifoline(732-50-3)
Safety Data
1. Hazard Codes: N/A
2. Statements: N/A
3. Safety Statements: N/A
4. WGK Germany:
5. RTECS:
6. HazardClass: N/A
7. PackingGroup: N/A
8. Hazardous Substances Data: 732-50-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 732-50-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 732-50:
(5*7)+(4*3)+(3*2)+(2*5)+(1*0)=63
63 % 10 = 3
So 732-50-3 is a valid CAS Registry Number.

InChI:InChI=1/C15H20N2O2/c18-12-4-5-16-8-10-6-11(14(16)7-12)9-17-13(10)2-1-3-15(17)19/h1-3,10-12,14,18H,4-9H2/t10-,11-,12+,14-/m1/s1

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