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(1R,2S,12R,13R)-12-hydroxy-4,8,12-trimethyl-16-methylidene-15-oxo-14-oxabicyclo[11.3.1]heptadeca-4,8-dien-2-yl acetate is a complex organic molecule with a bicyclic structure, featuring a hydroxyl group, a methylidene group, and an acetate group. It consists of 17 carbon atoms and is distinguished by its unique arrangement of double bonds and functional groups. (1R,2S,12R,13R)-12-hydroxy-4,8,12-trimethyl-16-methylidene-15-oxo-14-oxabicyclo[11.3.1]heptadeca-4,8-dien-2-yl acetate's specific stereochemistry is denoted by the (1R,2S,12R,13R) configuration, which describes the spatial orientation of its chiral centers.

28028-68-4

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28028-68-4 Usage

Uses

Used in Pharmaceutical Research:
(1R,2S,12R,13R)-12-hydroxy-4,8,12-trimethyl-16-methylidene-15-oxo-14-oxabicyclo[11.3.1]heptadeca-4,8-dien-2-yl acetate is utilized as a research compound for the development of new pharmaceuticals. Its complex structure and functional groups make it a promising candidate for the synthesis of novel drug molecules.
Used in Chemical Research:
In the field of chemical research, (1R,2S,12R,13R)-12-hydroxy-4,8,12-trimethyl-16-methylidene-15-oxo-14-oxabicyclo[11.3.1]heptadeca-4,8-dien-2-yl acetate serves as a valuable compound for studying the properties and reactivity of complex organic molecules. Its unique arrangement of functional groups allows for exploration of various chemical reactions and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 28028-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28028-68:
(7*2)+(6*8)+(5*0)+(4*2)+(3*8)+(2*6)+(1*8)=114
114 % 10 = 4
So 28028-68-4 is a valid CAS Registry Number.

28028-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Crassin acetate

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:28028-68-4 SDS

28028-68-4Relevant academic research and scientific papers

Synthesis of analogues of Eunicea γ-cembranolides containing cyclic ethers via saponification

Rodriguez,Pina,Acosta,Ramirez,Soto

, p. 648 - 658 (2001)

A method for the synthesis of derivatives of the lead structures euniolide (1), 12,13-bisepieupalmerin (2), and eupalmerin acetate (3) containing tetrahydrofuran and tetrahydropyran ring systems was developed on the basis of alkali-induced intramolecular oxacyclizations. Representatives of the new analogues were submitted to the in vitro antitumor cell-line-screening program of the National Cancer Institute (NCI). While it was shown that a variety of structural modifications are possible, these transformations led typically to nontoxic synthetic cembranoids.

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