63215-31-6 Usage
General Description
6-Isopropoxy-3,4-dihydro-2h-naphthalen-1-one, also known as Galaxolide, is a synthetic fragrance compound commonly used in a wide variety of scented consumer products. It is a member of the musk fragrance family and is known for its sweet, floral, and woody aroma. Galaxolide is often used in perfumes, colognes, deodorants, soaps, and other personal care products to impart a long-lasting, pleasant scent. It is considered to be a safe ingredient for use in cosmetics and personal care products and is approved for use in various countries around the world. However, like many synthetic fragrance compounds, there is ongoing research into its potential environmental and health effects.
Check Digit Verification of cas no
The CAS Registry Mumber 63215-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,1 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63215-31:
(7*6)+(6*3)+(5*2)+(4*1)+(3*5)+(2*3)+(1*1)=96
96 % 10 = 6
So 63215-31-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O2/c1-9(2)15-11-6-7-12-10(8-11)4-3-5-13(12)14/h6-9H,3-5H2,1-2H3
63215-31-6Relevant articles and documents
4,5-DIHYDRONAPHTHO [1,2-b] THIOPHENE DERIVATIVE
-
Page/Page column 18, (2010/11/08)
A 4,5-dihydronaphtho[1,2-b]thiophene derivative expressed by the formula: (wherein R1 is a C1 to C10 1-hydroxyalkyl group or a C1 to C10 acyl group, and R2 and R3 separately substitute in the 6-, 7-, 8-, or 9-positions, and are each independently a hydrogen atom, a halogen atom, a C1 to C10 alkyl group, a hydroxy group, a C1 to C10 alkoxy group, a C1 to C5 alkenyloxy group, a C1 to C5 alkynyloxy group, a benzyloxy group, or the like, provided that when R1 is an acyl group and R2 is a hydrogen atom, then R3 is neither a hydrogen atom nor an acetyl group), or a pharmaceutically acceptable salt thereof. This is a novel compound that is effective in reducing triglyceride levels in the liver and reducing blood glucose levels.
A new access to 1-naphthylamines by an equivalent Semmler-Wolff reaction
Janin,Bisagni
, p. 57 - 59 (2007/10/02)
A new access to 1-naphthylamines from the corresponding 3,4-dihydro-1(2H)-naphthalenones (α-tetralones) is described. It proceeds in a two-step sequence: preparation of the benzyl Schiff's base of an α-tetralone followed by aromatization over palladium ca
