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(4R)-4-(3-Furyl)-1,4,4a,5,6,6aβ,7,8,9,10,11,12-dodecahydro-4aβ,7,9,9-tetramethyl-2,10,13-trioxo-7β,11β-methano-2H-cycloocta[f][2]benzopyran-8β-acetic acid methyl ester is a complex organic molecule characterized by a cyclooctane-fused coumarin structure. It features a methyl ester functional group and is composed of multiple interconnected rings and side chains. (4R)-4-(3-Furyl)-1,4,4a,5,6,6aβ,7,8,9,10,11,12-dodecahydro-4aβ,7,9,9-tetramethyl-2,10,13-trioxo-7β,11β-methano-2H-cycloocta[f][2]benzopyran-8β-acetic acid methyl ester has several chiral centers, which confer a specific stereochemistry, designated as (4R). Its intricate chemical structure suggests potential pharmaceutical or biological activity, making it a promising candidate for further research in medicinal chemistry or drug development.

1915-67-9

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1915-67-9 Usage

Uses

Used in Pharmaceutical Industry:
(4R)-4-(3-Furyl)-1,4,4a,5,6,6aβ,7,8,9,10,11,12-dodecahydro-4aβ,7,9,9-tetramethyl-2,10,13-trioxo-7β,11β-methano-2H-cycloocta[f][2]benzopyran-8β-acetic acid methyl ester is used as a potential pharmaceutical agent for its possible biological activity. (4R)-4-(3-Furyl)-1,4,4a,5,6,6aβ,7,8,9,10,11,12-dodecahydro-4aβ,7,9,9-tetramethyl-2,10,13-trioxo-7β,11β-methano-2H-cycloocta[f][2]benzopyran-8β-acetic acid methyl ester's unique structure and chiral centers may contribute to its interaction with biological targets, offering opportunities for the development of new drugs or therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (4R)-4-(3-Furyl)-1,4,4a,5,6,6aβ,7,8,9,10,11,12-dodecahydro-4aβ,7,9,9-tetramethyl-2,10,13-trioxo-7β,11β-methano-2H-cycloocta[f][2]benzopyran-8β-acetic acid methyl ester serves as a subject for further investigation to elucidate its potential pharmacological properties. Researchers may explore its binding affinity to various receptors, enzymes, or other biological targets, as well as its potential to modulate specific signaling pathways or biological processes.
Used in Drug Development:
(4R)-4-(3-Furyl)-1,4,4a,5,6,6aβ,7,8,9,10,11,12-dodecahydro-4aβ,7,9,9-tetramethyl-2,10,13-trioxo-7β,11β-methano-2H-cycloocta[f][2]benzopyran-8β-acetic acid methyl ester may be utilized in drug development as a lead compound. Its complex structure and stereochemistry could be optimized through medicinal chemistry techniques to enhance its potency, selectivity, and pharmacokinetic properties, ultimately leading to the creation of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1915-67-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1915-67:
(6*1)+(5*9)+(4*1)+(3*5)+(2*6)+(1*7)=89
89 % 10 = 9
So 1915-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H32O7/c1-25(2)19(12-20(28)32-5)27(4)17-6-8-26(3)18(15(17)10-16(22(25)30)23(27)31)11-21(29)34-24(26)14-7-9-33-13-14/h7,9,13,16-17,19,24H,6,8,10-12H2,1-5H3/t16-,17+,19+,24+,26-,27+/m1/s1

1915-67-9SDS

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 Mexicanolide

1.2 Other means of identification

Product number -
Other names (1R,4S)-p-menthan-3-one

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:1915-67-9 SDS

1915-67-9Downstream Products

1915-67-9Relevant academic research and scientific papers

Enantioselective total synthesis of the mexicanolides: Khayasin, proceranolide, and mexicanolide

Faber, Jonathan M.,Eger, Wilhelm A.,Williams, Craig M.

, p. 8913 - 8921 (2013/01/15)

The enantioselective total synthesis of the limonoids khayasin, proceranolide and mexicanolide was achieved via a convergent strategy utilizing a tactic aimed at incorporating natural products as advanced intermediates. This extended biomimetically inspir

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