Alstovenine is a naturally occurring chemical compound found in the plant Alstonia venenata, which is traditionally used in Chinese medicine. It belongs to the class of indole alkaloids and is known for its potential pharmacological properties, such as anti-inflammatory and anti-cancer effects. The compound has been the subject of scientific research to explore its therapeutic potential and understand its mechanisms of action. Alstovenine's structure and biological activities make it an interesting candidate for further study in the development of new drugs and treatments.

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Basic information
1. Product Name: Alstovenine
2. Synonyms: Alstovenine;(20α)-17β-Hydroxy-9-methoxyyohimban-16β-carboxylic acid methyl ester;3-Isovenenatine
3. CAS NO:4837-79-0
4. Molecular Formula: C22H28N2O4
5. Molecular Weight: 384.46872
6. EINECS: N/A
7. Product Categories: N/A
8. Mol File: 4837-79-0.mol
Chemical Properties
1. Melting Point: 169-171 °C
2. Boiling Point: 571.3°C at 760 mmHg
3. Flash Point: 299.3°C
4. Appearance: /
5. Density: 1.32g/cm³
6. Vapor Pressure: 6.86E-14mmHg at 25°C
7. Refractive Index: 1.647
8. Storage Temp.: N/A
9. Solubility: N/A
10. PKA: 14.39±0.40(Predicted)
11. CAS DataBase Reference: Alstovenine(CAS DataBase Reference)
12. NIST Chemistry Reference: Alstovenine(4837-79-0)
13. EPA Substance Registry System: Alstovenine(4837-79-0)
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: 4837-79-0(Hazardous Substances Data)

4837-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4837-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4837-79:
(6*4)+(5*8)+(4*3)+(3*7)+(2*7)+(1*9)=120
120 % 10 = 0
So 4837-79-0 is a valid CAS Registry Number.

InChI:InChI=1/C22H28N2O4/c1-27-18-5-3-4-15-19(18)13-8-9-24-11-12-6-7-17(25)20(22(26)28-2)14(12)10-16(24)21(13)23-15/h3-5,12,14,16-17,20,23,25H,6-11H2,1-2H3/t12-,14+,16+,17-,20+/m1/s1

4837-79-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	alstovenine

1.2 Other means of identification

Product number	-
Other names	Isovenantin

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4837-79-0 SDS

4837-79-0Upstream product

1055-75-0 venenatine

4837-79-0Downstream Products

4837-79-0Relevant articles and documents

3,4-Bond Cleavage of Tetrahydro-β-Carboline Alkaloids: Transformation of Venenatine and Rhazine to the Corresponding 2-Acylindole Derivatives

Banerji, Avijit,Siddhanta, Arup K

, p. 542 - 547 (2007/10/02)

3,4-Bond cleavage reactions of venenatine (1) and rhazine (6) with cyanogen bromide in ethanolic chloroform were studied.The resulting seco-bases were transformed to the corresponding 2-acylindoles with t-BuOCl.

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CAS

4837-79-0