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The chemical compound "(3R,5S,6'aS,10'aR)-5-(3-Furyl)-4,5,6',6'aβ-tetrahydro-8'α-methylspiro[furan-3(2H),7'(8'H)-naphtho[1,8a-c]furan]-2,3',10'(5'H,9'H)-trione" is a complex, chiral molecule with a unique structure. It features a spiro-fused system, which connects a furan ring to a naphtho-furan ring. The compound is characterized by its tetrahydro nature, indicating the presence of four hydrogen atoms in a cyclic structure. The molecule also includes a methyl group at the 8'α position, which contributes to its stereochemistry. The compound's name reflects its specific arrangement of atoms and functional groups, with the R and S configurations at various carbon centers, and the presence of a trione group, indicating three carbonyl groups. This intricate structure is likely to have specific applications in fields such as organic chemistry, pharmaceuticals, or materials science, where the stereochemistry and functional groups play crucial roles in the compound's properties and potential interactions.

76902-35-7

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76902-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76902-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,0 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76902-35:
(7*7)+(6*6)+(5*9)+(4*0)+(3*2)+(2*3)+(1*5)=147
147 % 10 = 7
So 76902-35-7 is a valid CAS Registry Number.

76902-35-7SDS

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 teuscordinone

1.2 Other means of identification

Product number -
Other names teuscordinon

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:76902-35-7 SDS

76902-35-7Downstream Products

76902-35-7Relevant academic research and scientific papers

Some chemical transformations of the neo-clerodane diterpene teubotrin

Malakov,De la Torre,Rodriguez,Papanov

, p. 10129 - 10136 (1991)

Starting from the natural neo-clerodane diterpenoid teubotrin (1) several neo-clerodane derivatives (3-7, 9-11) have been obtained. The naturally occurring diterpenoid teuscordinon (12) has also been synthesized from teubotrin (1), showing thereby how some of these transformation can be useful for the synthesis of other natural neo-clerodane diterpenes. The latter are of interest due to their activity as insect antifeedants and other important biological properties.

6-β-Hydroxyteuscordin and 2β-,6β-Dihydroxyteuscordin Two New Diterpenoids from Teucrium scordium L.

Papanov, Georgi Y.,Malakov, Peter Y.

, p. 519 - 520 (2007/10/02)

Two new furanoid diterpenes of clerodane type, 6β-hydorxyteuscordin (1) and 2β,6β-dihydroxyteuscordin (3) have been isolated from Teucrium scordium var. scordium, Lamiaceae.Their structures and stereochemistry have been determined on the basis of chemical reactions and spectroscopic evidense. - Key words: Teucrium scordium L., Lamiaceae, Clerodane Type, Furanoid diterpene

New Furanoid Diterpenes from Teucrium scordium L.

Papanov, Georgi Y.,Malakov, Peter Y.

, p. 112 - 113 (2007/10/02)

Two new furanoid diterpenes of clerodane type, 6-ketoteuscordin (1) and 6α-hydroxyteuscordin (2) have been isolated from Teucrium scordium var. scordium, Lamiaceae.Their structures and stereochemistry have been determined. - Keywords: Teucrium scordium L., Lamiaceae, Clerodane Type, Furanoid Diterpene, 6-Ketoteuscordin

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