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74690-89-4

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74690-89-4 Usage

Description

3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is a complex organic molecule that consists of a mixture of 3-methyl-2-butenoic acid and an ester formed from a hydroxy compound and a carboxylic acid. 3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester features a vinyl group, a cycloheptene ring, and a pentenyl group, which contribute to its unique structure and potential reactivity. Its intricate composition suggests that it may possess specific properties that could be of interest to researchers and chemists in various fields, including pharmaceuticals and fragrances.

Uses

Used in Pharmaceutical Industry:
3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is used as a pharmaceutical compound for its potential therapeutic applications. Its complex structure may offer unique interactions with biological systems, making it a candidate for the development of new drugs or drug delivery systems.
Used in Fragrance Industry:
In the fragrance industry, 3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is used as a scent ingredient. Its specific chemical composition may contribute to the creation of novel fragrances or enhance existing ones, providing a distinct olfactory profile.
Used in Chemical Research:
3-Methyl-2-butenoic acid [2-[5-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-6-oxo-7-(2-oxopropyl)-4-cyclohepten-1-yl]vinyl] ester is utilized in chemical research as a subject of study for its unique structural features and potential reactivity. Researchers may explore its properties to gain insights into new chemical reactions or to develop innovative applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 74690-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,9 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74690-89:
(7*7)+(6*4)+(5*6)+(4*9)+(3*0)+(2*8)+(1*9)=164
164 % 10 = 4
So 74690-89-4 is a valid CAS Registry Number.

74690-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Vibsanin C

1.2 Other means of identification

Product number -
Other names -

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:74690-89-4 SDS

74690-89-4Upstream product

74690-89-4Downstream Products

74690-89-4Relevant articles and documents

Absolute structure of vibsanins B and C, and their chemical correlation

Fukuyama, Yoshiyasu,Minami, Hiroyuki,Takaoka, Shigeru,Kodama, Mitsuaki,Kawazu, Kazuyoshi,Nemoto, Hisao

, p. 1435 - 1438 (1997)

The absolute structure of vibsanin C, a novel 7-membered vibsane-type diterpene isolated from the leaves of Viburnum awabuki, has been established by X-ray crystallographic analysis of its derivative. Vibsanin C has been proved to be one of Cope rearranged products from vibsanin B, a 11-membered vibsane-type diterpene.

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