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6-Propyl-2-methoxynaphthalene is a chemical compound that features a naphthalene molecule with a propyl group and a methoxy group attached to it. It is recognized for its sweet, floral, and woody odor profile, which makes it a valuable component in the fragrance industry.

94134-18-6

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94134-18-6 Usage

Uses

Used in Fragrance Industry:
6-Propyl-2-methoxynaphthalene is used as a fragrance ingredient for its pleasant and long-lasting scent. It is incorporated into various products such as perfumes, soaps, and other personal care items due to its appealing odor profile.
Used in Food Industry:
6-PROPYL-2-METHOXYLNAPHTHALINE also serves as a flavoring agent in food products, enhancing the taste and aroma of various culinary creations.
Used in Pest Control:
6-Propyl-2-methoxynaphthalene is utilized as an insect attractant, making it a component in pest control strategies to lure and manage insect populations.
It is crucial to handle 6-Propyl-2-methoxynaphthalene with care due to its potential to cause irritation to the skin, eyes, and respiratory system if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 94134-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,3 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94134-18:
(7*9)+(6*4)+(5*1)+(4*3)+(3*4)+(2*1)+(1*8)=126
126 % 10 = 6
So 94134-18-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O/c1-3-4-11-5-6-13-10-14(15-2)8-7-12(13)9-11/h5-10H,3-4H2,1-2H3

94134-18-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-PROPYL-2-METHOXYLNAPHTHALINE

1.2 Other means of identification

Product number -
Other names 2-PROPYL-6-METHOXYNAPHTHALENE

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:94134-18-6 SDS

94134-18-6Relevant academic research and scientific papers

NOVEL LIQUID CRYSTALLINE COMPOUND AND LIQUID CRYSTAL COMPOSITION PREPARED USING THE SAME

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Paragraph 0209; 0210, (2016/10/07)

PROBLEM TO BE SOLVED: To provide a liquid crystal compound that has a low viscosity, a high isotropic transition temperature, a high compatibility, and a high refractive index anisotropy, and is also resistant to degradation due to heat and light. SOLUTION: The present invention illustrates a naphthalene derivative represented by the general formula (1), specifically, for example, a naphthalene derivative obtained through a reaction represented by the following formula, as well as a liquid crystal composition comprising the same. Use of the liquid crystal composition comprising the liquid crystal compound makes it possible to provide a high-speed response liquid crystal display element. COPYRIGHT: (C)2016,JPOandINPIT

Naphthalene derivative and liquid crystal composition comprising the same

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, (2008/06/13)

Disclosed is a novel liquid-crystalline compound which is a naphthalene derivative useful as an electro-optical liquid crystal display material, a liquid crystal composition containing such naphthalene derivatives and a liquid crystal display device comprising the same. The naphthalene derivative provided by the present invention exhibits an excellent liquid-crystallinity and miscibility with currently widely used liquid crystal compositions or compositions. The addition of the naphthalene derivative makes it possible to drastically lower the threshold voltage of the liquid crystal composition while maintaining its high response. The naphthalene derivative of the present invention is characterized by a large birefringence index. Further, most of the naphthalene derivative of the present invention has no strongly polar group in its molecule and thus can also be used for active matrix driving. Moreover, as shown in the foregoing examples, the naphthalene derivative of the present invention can be easily produced and is colorless and chemically stable. Accordingly, the liquid crystal composition comprising the naphthalene derivative of the present invention is extremely useful as a practical liquid crystal composition, particularly a liquid crystal composition which can operate within a wide temperature range and requires a high speed response and a low voltage driving.

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