7382-37-8 Usage
General Description
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. 1-(METHOXYMETHOXY)NAPHTHALENE is often used as a fragrance ingredient in various consumer products such as cosmetics, perfumes, and air fresheners. It is also used in the production of flavors and fragrances. However, 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.
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
7382-37-8Relevant articles and documents
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.
