Acetamide,N-1-naphthalenyl- (575-36-0)

The N-Acetyl-1-aminonaphthalene, with CAS registry number 575-36-0, belongs to the following product categories: (1)Intermediates of Dyes and Pigments; (2)Auxins; (3)Biochemistry; (4)Plant Growth Regulators; (5)Pesticide Intermediate. Its systematic name and its IUPAC name are the same, which is N-(naphthalen-1-yl)acetamide. When use this chemical, avoid contact with skin and eyes.

Physical properties of N-Acetyl-1-aminonaphthalene: (1)ACD/LogP: 2.31; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.31; (4)ACD/LogD (pH 7.4): 2.31; (5)ACD/BCF (pH 5.5): 33.73; (6)ACD/BCF (pH 7.4): 33.73; (7)ACD/KOC (pH 5.5): 431.88; (8)ACD/KOC (pH 7.4): 431.89; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 20.31 Å²; (13)Index of Refraction: 1.667; (14)Molar Refractivity: 58.36 cm³; (15)Molar Volume: 156.6 cm³; (16)Polarizability: 23.13×10^-24cm³; (17)Surface Tension: 49.2 dyne/cm; (18)Enthalpy of Vaporization: 66.65 kJ/mol; (19)Vapour Pressure: 4.73E-07 mmHg at 25°C.

Preparation: this chemical can be prepared by 1-[1]naphthyl-ethanone oxime. This reaction will need reagents phosphorus pentachloride, petroleum ether.

Uses of N-Acetyl-1-aminonaphthalene: it can be used to produce N-(4-bromo-[1]naphthyl)-acetamide. This reaction will need reagent N-bromosuccinimide and solvent CCl₄. The reaction time is 45 min. The yield is about 80%.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(Nc2cccc1ccccc12)C
(2)InChI: InChI=1/C12H11NO/c1-9(14)13-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3,(H,13,14)
(3)InChIKey: OKQIEBVRUGLWOR-UHFFFAOYAK
(4)Std. InChI: InChI=1S/C12H11NO/c1-9(14)13-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3,(H,13,14)
(5)Std. InChIKey: OKQIEBVRUGLWOR-UHFFFAOYSA-N