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1(4H)-Naphthalenone, 4a,5,6,7,8,8a-hexahydro-4a,8,8-trimethyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130894-45-0

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130894-45-0 Usage

Chemical Structure

Cyclic ketone compound with a naphthalene ring

Stereochemistry

transform with specific arrangement of atoms

Usage

Fragrance ingredient in soaps, detergents, perfumes, and cosmetics

Scent

Floral, fresh, and citrus-like

Aesthetic Purpose

To give products a pleasant aroma

Potential Side Effect

May cause skin irritation or allergic reactions in some individuals

Check Digit Verification of cas no

The CAS Registry Mumber 130894-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,9 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130894-45:
(8*1)+(7*3)+(6*0)+(5*8)+(4*9)+(3*4)+(2*4)+(1*5)=130
130 % 10 = 0
So 130894-45-0 is a valid CAS Registry Number.

130894-45-0Downstream Products

130894-45-0Relevant academic research and scientific papers

DIASTEREOCONTROLLED SYNTHESIS OF FUNCTIONALIZED TRANS-DECALINS VIA ELECTROCYCLIC REACTION OF TRIENOL ETHERS

Fehr, Charles,Galindo, Jose,Guntern, Olivier

, p. 4021 - 4024 (2007/10/02)

(E)-Trienol silyl ethers 10 and 11, selectively prepared by mono-Grignard reaction on methyl β-cyclogeranate (7) or by deprotonation of enone 8 were transformed to trans-decalins 5 and 6 by a thermal electrocyclic reaction.The hithero unknown enones 5 and 6 exhibit interesting organoleptic properties and show promise as versatile synthetic intermediates.The herein described transformation opens a new route for the direct construction of C(6)-functionalized drimanes such as cinnamodial (3) and forskolin (4).

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