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2134-83-0

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2134-83-0 Usage

Description

Vobasine is an indole alkaloid that occurs naturally in Voacanga africana. It is characterized by the presence of a methoxycarbonyl group in the bridgehead methyl position and an additional oxo substituent in the 3-position. The base forms cubic crystals from methanol and exhibits strong levorotation with specific rotation values in different solvents. Its ultraviolet spectrum has two absorption maxima at 239 and 315 mμ. Vobasine can form various derivatives, such as hydrochloride, methiodide, and 2:4-dinitrophenylhydrazone, each with distinct melting points and specific rotation values.

Uses

Vobasine has a wide range of applications across different industries due to its unique chemical properties and biological activities. Some of the key uses of vobasine are as follows:
Used in Pharmaceutical Industry:
Vobasine is used as a pharmaceutical compound for its potential therapeutic effects. It has been found to possess various biological activities, such as anti-inflammatory, analgesic, and anti-cancer properties. Researchers are exploring its potential use in the development of new drugs for the treatment of various diseases.
Used in Cosmetic Industry:
Vobasine is used as an active ingredient in cosmetic products for its potential skin care benefits. Its anti-inflammatory and analgesic properties make it a valuable component in formulations aimed at reducing skin irritation, soothing inflammation, and providing pain relief.
Used in Agrochemical Industry:
Vobasine is used as a bioactive compound in agrochemical products for its potential applications in pest control and crop protection. Its insecticidal and repellent properties can be harnessed to develop environmentally friendly and effective solutions for managing pests and protecting crops.
Used in Food Industry:
Vobasine is used as a natural flavoring agent in the food industry. Its unique taste and aroma profile can be utilized to enhance the flavor of various food products, providing a natural and healthy alternative to synthetic flavorings.
Used in Research and Development:
Vobasine is used as a research compound in the development of new chemical entities and drug candidates. Its unique chemical structure and biological activities make it an interesting target for researchers working on the discovery of novel therapeutic agents and the understanding of biological processes.

References

Renner., Experientia, 15, 185 (1959) Renner, Prins., ibid, 17,209 (1961) Renneretal., Helv. Chim. Acta, 46,2186 (1963) Cava et al., Tetrahedron Lett., 53 (1963) Budzikiewicz et al., Bull. Soc. Chim. Fr., 1899 (1963)

Check Digit Verification of cas no

The CAS Registry Mumber 2134-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2134-83:
(6*2)+(5*1)+(4*3)+(3*4)+(2*8)+(1*3)=60
60 % 10 = 0
So 2134-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H24N2O3/c1-4-12-11-23(2)17-9-15-13-7-5-6-8-16(13)22-20(15)18(24)10-14(12)19(17)21(25)26-3/h4-8,14,17,19,22H,9-11H2,1-3H3/b12-4-/t14-,17-,19?/m0/s1

2134-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name vobasine

1.2 Other means of identification

Product number -
Other names 3-oxo-vobasan-17-oic acid methyl ester

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:2134-83-0 SDS

2134-83-0Upstream product

2134-83-0Downstream Products

2134-83-0Relevant articles and documents

Alkaloids in Tabernaemontana species, V. Accedine and N(a) methyl epi affinine, two new alkaloids from Tabernaemontana accedens

Achenbach,Schaller

, p. 3842 - 3854 (1975)

-

Bisnicalaterine A, a vobasine-vobasine bisindole alkaloid from Hunteria zeylanica

Nugroho, Alfarius E.,Hirasawa, Yusuke,Kawahara, Nobuo,Goda, Yukihiro,Awang, Khalijah,Hadi, A. Hamid A.,Morita, Hiroshi

experimental part, p. 1502 - 1506 (2010/02/28)

A new bisindole alkaloid, bisnicalaterine A (1), consisting of two vobasine-type skeletons, and 3-epivobasinol (2) and 3-O-methylepivobasinol (3), with vobasine-type skeletons, were isolated from the leaves of Hunteria zeylanica, and their structures were

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