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1(2H)-Naphthalenone, 3,4-dihydro-6-octylis a synthetic organic compound with the molecular formula C18H24O. It is a pale yellow to brownish liquid characterized by a strong, musky odor. This chemical compound is known for its skin sensitizing properties, which necessitates caution in its use and adherence to safety guidelines to protect human health and the environment.

945632-75-7

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945632-75-7 Usage

Uses

Used in Personal Care Industry:
1(2H)-Naphthalenone, 3,4-dihydro-6-octylis used as a fragrance ingredient for its strong, musky odor, adding a distinctive scent to various personal care products such as perfumes, lotions, and soaps. Its unique aroma enhances the sensory experience of these products, making them more appealing to consumers.
Used in Insect Repellent Industry:
In the insect repellent industry, 1(2H)-Naphthalenone, 3,4-dihydro-6-octylis utilized for its ability to deter insects. Its strong odor serves as a natural deterrent, helping to keep insects at bay and providing protection against bites and discomfort.
Used in Food Industry:
As a flavoring agent, 1(2H)-Naphthalenone, 3,4-dihydro-6-octylis employed in the food industry to impart a unique taste and aroma to certain food products. Its distinct musky flavor can add depth and complexity to the taste profiles of various culinary creations.

Check Digit Verification of cas no

The CAS Registry Mumber 945632-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 945632-75:
(8*9)+(7*4)+(6*5)+(5*6)+(4*3)+(3*2)+(2*7)+(1*5)=197
197 % 10 = 7
So 945632-75-7 is a valid CAS Registry Number.

945632-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-octyl-3,4-dihydro-2H-naphthalen-1-one

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:945632-75-7 SDS

945632-75-7Relevant academic research and scientific papers

Stereochemistry-activity relationship of orally active tetralin S1P agonist prodrugs

Ma, Bin,Guckian, Kevin M.,Lin, Edward Yin-Shiang,Lee, Wen-Cherng,Scott, Daniel,Kumaravel, Gnanasambandam,Macdonald, Timothy L.,Lynch, Kevin R.,Black, Cheryl,Chollate, Sowmya,Hahm, Kyungmin,Hetu, Gregg,Jin, Ping,Luo, Yi,Rohde, Ellen,Rossomando, Anthony,Scannevin, Robert,Wang, Joy,Yang, Chunhua

scheme or table, p. 2264 - 2269 (2010/07/05)

Modifying FTY720, an immunosuppressant modulator, led to a new series of well phosphorylated tetralin analogs as potent S1P1 receptor agonists. The stereochemistry effect of tetralin ring was probed, and (-)-(R)-2-amino-2-((S)-6-octyl-1,2,3,4-tetrahydrona

BICYCLIC SPHINGOSINE 1-PHOSPHATE ANALOGS

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, (2009/04/25)

Compounds that have agonist activity at one or more of the SlP receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at SlP receptors. Formula (I):

BICYCLIC SPHINGOSINE 1-PHOSPHATE ANALOGS

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Page/Page column 30, (2008/06/13)

Compounds that have agonist activity at one or more of the S1P receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at S1P receptors.

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