Nerolin Yara Yara

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Product Description

Nerolin yara yara 's cas code is 93-04-9.

Nerolin yara yara Basic information

Nerolin yara yara Chemical Properties

Melting point	70-73 °C(lit.)
Boiling point	274 °C(lit.)
density	1.064 g/mL at 25 °C(lit.)
FEMA	4704 \| BETA-NAPHTHYL METHYL ETHER
refractive index	1.5440 (estimate)
Fp	272-274°C
storage temp.	Store below +30°C.
solubility	H2O: soluble (completely)
form	Crystalline Solid
color	White to yellow-brown
Water Solubility	INSOLUBLE
JECFA Number	1257
Merck	14,5997
BRN	1859408
Stability:	Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey	LUZDYPLAQQGJEA-UHFFFAOYSA-N
CAS DataBase Reference	93-04-9(CAS DataBase Reference)
NIST Chemistry Reference	Naphthalene, 2-methoxy-(93-04-9)
EPA Substance Registry System	Naphthalene, 2-methoxy- (93-04-9)

Nerolin yara yara Safety Information

Nerolin yara yara Usage And Synthesis

Description	β-Naphthyl methyl ether has an intensely sweet, floral odor suggestive of orange blossoms. It is free from naphthol by-odor. It has a sweet, strawberry taste. This may be prepared from potassium β-naphthol and methyl chloride at 300°C; by methylation of β-naphthol with dimethyl sulfate or by direct esterification with methyl alcohol.
Chemical Properties	β-Naphthyl methyl ether has an intensely sweet, floral odor suggestive of orange blossoms; free from naphthol by-odor. It has a sweet, strawberry taste
Chemical Properties	white powder
Chemical Properties	Methyl 2-Naphthyl Ether forms white crystals (mp 73–74°C) with an intense orange blossom odor.
Uses	2-Methoxynaphthalene is an Impurity of the non-steroidal anti-inflammatory Naproxen (N377525).
Preparation	From postassium β-naphthol and methyl chloride at 300°C; by methylation of β-naphthlol with dimethyl sulfate or by direct esterification with methyl alcohol
Purification Methods	Fractionally distil the ether under vacuum. Crystallise it from absolute EtOH, aqueous EtOH, *C6H6, pet ether or n-heptane, and dry it under vacuum in an Abderhalden pistol or distil it in vacuo. The picrate has m 118o (from EtOH or CHCl3). [Kikuchi et al. J Phys Chem 91 574 1987, Beilstein 6 III 2969, 6 IV 4257.]

2-Methoxynaphthalene Preparation Products And Raw materials

Raw materials	Methanol-->Sulfuric acid-->1-Aminonaphthalene-->Aurantiol (methyl anthranilate and hydroxycitronellal schiff base)
Preparation Products	2-Acetyl-6-methoxynaphthalene-->DL-6-METHOXY-ALPHA-METHYL-2-NAPHTHALENEMETHANOL-->6-METHOXY-2-NAPHTHOIC ACID-->6-Methoxy-2-naphthaldehyde-->6-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE