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1-(Methoxymethoxy)naphthalene, also known as methoxymethoxy-1-naphthalene, is a chemical compound with the molecular formula C13H12O2. It is a white solid with a molecular weight of 200.23 g/mol.
Used in Fragrance Industry:
1-(Methoxymethoxy)naphthalene is used as a fragrance ingredient for its aromatic properties in various consumer products such as cosmetics, perfumes, and air fresheners.
Used in Flavor and Fragrance Production:
1-(Methoxymethoxy)naphthalene is used in the production of flavors and fragrances, contributing to the unique scents and tastes in various products.
It is important to handle this chemical with care as it may cause irritation to the skin, eyes, and respiratory tract upon prolonged exposure. Additionally, it may be harmful if ingested and can pose a risk to aquatic life. Therefore, proper safety measures should be taken when handling 1-(methoxymethoxy)naphthalene.

7382-37-8

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7382-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7382-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7382-37:
(6*7)+(5*3)+(4*8)+(3*2)+(2*3)+(1*7)=108
108 % 10 = 8
So 7382-37-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O2/c1-13-9-14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,9H2,1H3

7382-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Methoxymethoxy)naphthalene

1.2 Other means of identification

Product number -
Other names REELDIWIMZYNLC-UHFFFAOYSA

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:7382-37-8 SDS

7382-37-8Relevant academic research and scientific papers

EXCEPTIONAL REACTIVITY OF THE AROMATIC RING IN 8-SUBSTITUTED 1-NAPHTHOL DERIVATIVES. READY REDUCTION TO TETRALINS.

Kirby, Anthony J.,Percy, Jonathan M.

, p. 6911 - 6920 (2007/10/02)

8-Lithio-1-methoxynaphthalene is acylated and alkylated to give 8-CO2H, COCH3 and Me2C(OH) derivatives in only poor yields.Methyl lithium does not add to the 8-acetyl compound, converting it instead to the lithium enolate.Compounds with secondary or tertiary alkyl peri-substituents undergo rapid protodealkylation, and are readily reduced to tetralins by H2/Pd at atmospheric pressure.

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