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2(1H)-Naphthalenone, octahydro-4,4a-dimethyl-6-(1-methylethenyl)-, (4R,4aS,6R,8aS)is an organic compound with a unique molecular structure characterized by its octahydro-naphtholone core and various substituents. It is known for its distinct citrus-like, green odor, which makes it a valuable component in the fragrance industry.

20489-53-6

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20489-53-6 Usage

Uses

Used in Fragrance Industry:
2(1H)-Naphthalenone, octahydro-4,4a-dimethyl-6-(1-methylethenyl)-, (4R,4aS,6R,8aS)is used as a fragrance ingredient for its citrus-like, green odor. Its aroma threshold values make it a suitable candidate for creating various scents in the perfumery and cosmetics industry.
Used in Flavor Industry:
In addition to its application in the fragrance industry, 2(1H)-Naphthalenone, octahydro-4,4a-dimethyl-6-(1-methylethenyl)-, (4R,4aS,6R,8aS)can also be used as a flavoring agent. Its unique odor profile can be utilized to enhance the taste and aroma of various food and beverage products.
Used in Research and Development:
Due to its chemical properties and potential applications, 2(1H)-Naphthalenone, octahydro-4,4a-dimethyl-6-(1-methylethenyl)-, (4R,4aS,6R,8aS)may also be used in research and development for the synthesis of new compounds or the study of its properties in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 20489-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,8 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20489-53:
(7*2)+(6*0)+(5*4)+(4*8)+(3*9)+(2*5)+(1*3)=106
106 % 10 = 6
So 20489-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O/c1-10(2)12-5-6-13-8-14(16)7-11(3)15(13,4)9-12/h11-13H,1,5-9H2,2-4H3/t11-,12-,13+,15+/m1/s1

20489-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,4aS,6R,8aS)-4,4a-dimethyl-6-prop-1-en-2-yl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one

1.2 Other means of identification

Product number -
Other names Dihydronootkatone

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:20489-53-6 SDS

20489-53-6Downstream Products

20489-53-6Relevant academic research and scientific papers

Hydrogenation selectivity of the Bicyclo[4.4.0]decane ring system of valencanes

Sauer, Anne M.,Crowe, William E.,Henderson, Gregg,Laine, Roger A.

scheme or table, p. 445 - 448 (2010/04/26)

To test the selectivity of sterically hindered systems, (+)-nootkatone and derivatives were subjected to a wide variety of hydrogenation methodologies. The steric impact of the C-4 methyl substituent seems to be responsible for the inability of the system to adopt the cis-fused structure. Georg Thieme Verlag Stuttgart New York.

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