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3-(4-Methoxy-1-naphthyl)acrylic acid, also known as 4-Methoxy-1-naphthalenylacrylic acid, is a chemical compound with the molecular formula C14H12O3. It is a derivative of naphthalene and is often used as a building block in the synthesis of various functional organic molecules. 3-(4-METHOXY-1-NAPHTHYL)ACRYLIC ACID is commonly utilized in the fields of pharmaceuticals and organic chemistry, where it can be used as a starting material for the production of various pharmaceuticals and agrochemicals. It also has potential applications in the development of new materials and as a reagent in organic synthesis. Additionally, it is important to handle 3-(4-METHOXY-1-NAPHTHYL)ACRYLIC ACID with caution, as it may have potential risks to human health and the environment.

15971-30-9

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15971-30-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-Methoxy-1-naphthyl)acrylic acid is used as a starting material for the production of various pharmaceuticals. Its unique chemical structure allows for the synthesis of a wide range of bioactive compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(4-Methoxy-1-naphthyl)acrylic acid is used as a building block for the synthesis of various agrochemicals. Its versatile chemical properties enable the development of new compounds with improved efficacy and selectivity in crop protection.
Used in Material Science:
3-(4-Methoxy-1-naphthyl)acrylic acid has potential applications in the development of new materials. Its unique chemical structure can be utilized to create novel materials with specific properties, such as improved stability, enhanced reactivity, or tailored physical characteristics.
Used as a Reagent in Organic Synthesis:
In organic synthesis, 3-(4-Methoxy-1-naphthyl)acrylic acid serves as a valuable reagent. Its ability to participate in various chemical reactions, such as addition, substitution, and condensation, makes it a useful component in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 15971-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15971-30:
(7*1)+(6*5)+(5*9)+(4*7)+(3*1)+(2*3)+(1*0)=119
119 % 10 = 9
So 15971-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O3/c1-17-13-8-6-10(7-9-14(15)16)11-4-2-3-5-12(11)13/h2-9H,1H3,(H,15,16)/b9-7+

15971-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxynaphthalen-1-yl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-methoxy-[1]naphthyl)-acrylic acid

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:15971-30-9 SDS

15971-30-9Relevant academic research and scientific papers

Evaluation of synthetic naphthalene derivatives as novel chemical chaperones that mimic 4-phenylbutyric acid

Mimori, Seisuke,Koshikawa, Yukari,Mashima, Yu,Mitsunaga, Katsuyoshi,Kawada, Koichi,Kaneko, Masayuki,Okuma, Yasunobu,Nomura, Yasuyuki,Murakami, Yasuoki,Kanzaki, Tetsuto,Hamana, Hiroshi

, p. 811 - 814 (2015/02/19)

The chemical chaperone 4-phenylbutyric acid (4-PBA) has potential as an agent for the treatment of neurodegenerative diseases. However, the requirement of high concentrations warrants chemical optimization for clinical use. In this study, novel naphthalene derivatives with a greater chemical chaperone activity than 4-PBA were synthesized with analogy to the benzene ring. All novel compounds showed chemical chaperone activity, and 2 and 5 possessed high activity. In subsequent experiments, the protective effects of the compounds were examined in Parkinson's disease model cells, and low toxicity of 9 and 11 was related to amphiphilic substitution with naphthalene.

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