Acetamide,N-(2-nitr...

Acetamide,N-(2-nitrophenyl)-

Acetamide,N-(2-nitrophenyl)-

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Keywords

N-Acetyl-o-nitroaniline NSC 1313 o-Nitroacetanilide

Quick Details

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  • Application:The Acetamide,N-(2-nitrophenyl)-, with the CAS registry number 552-32-9 and EINECS registry number 209-009-6, has the systematic name of N-(2-nitrophenyl)acetamide. It belongs to the following product
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  • Transportation:The Acetamide,N-(2-nitrophenyl)-, with the CAS registry number 552-32-9 and EINECS registry number 209-009-6, has the systematic name of N-(2-nitrophenyl)acetamide. It belongs to the following product

Superiority:

The Acetamide,N-(2-nitrophenyl)-, with the CAS registry number 552-32-9 and EINECS registry number 209-009-6, has the systematic name of N-(2-nitrophenyl)acetamide. It belongs to the following product categories: Intermediates of Dyes and Pigments; Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts; Anilines, Amides & Amines; Nitro Compounds. And the molecular formula of the chemical is C8H8N2O3. What's more, it can be prepared by Acetic anhydride acetylation with ortho-nitroaniline. And it always used for the synthesis of dyes and other organic.

The characteristics of Acetamide,N-(2-nitrophenyl)- are as followings: (1)ACD/LogP: 1.00; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1; (4)ACD/LogD (pH 7.4): 1; (5)ACD/BCF (pH 5.5): 3.39; (6)ACD/BCF (pH 7.4): 3.39; (7)ACD/KOC (pH 5.5): 83.37; (8)ACD/KOC (pH 7.4): 83.37; (9)#H bond acceptors: 5; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 66.13 Å2; (13)Index of Refraction: 1.617; (14)Molar Refractivity: 47.07 cm3; (15)Molar Volume: 134.3 cm3; (16)Polarizability: 18.66×10-24cm3; (17)Surface Tension: 55.3 dyne/cm; (18)Density: 1.34 g/cm3; (19)Flash Point: 188.5 °C; (20)Enthalpy of Vaporization: 63.73 kJ/mol; (21)Boiling Point: 388.1 °C at 760 mmHg; (22)Vapour Pressure: 3.14E-06 mmHg at 25°C. 

Preparation of Acetamide,N-(2-nitrophenyl)-: This chemical can be prepared by acetic acid anhydride and 2-nitro-aniline. The reaction will need reagent Mg(ClO4)2. The reaction time is 0.5 hours with temperature of 20°C, and the yield is about 89%.

Uses of Acetamide,N-(2-nitrophenyl)-: It can react with 3-bromo-2-methyl-propene to produce o-nitro-N-(2-methyl-2-propenyl)acetanilide. This reaction will need reagent KOH, and the menstruum acetone. The reaction time is 3 minutes with heating, and the yield is about 92%.

Details:

The Acetamide,N-(2-nitrophenyl)-, with the CAS registry number 552-32-9 and EINECS registry number 209-009-6, has the systematic name of N-(2-nitrophenyl)acetamide. It belongs to the following product categories: Intermediates of Dyes and Pigments; Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts; Anilines, Amides & Amines; Nitro Compounds. And the molecular formula of the chemical is C8H8N2O3. What's more, it can be prepared by Acetic anhydride acetylation with ortho-nitroaniline. And it always used for the synthesis of dyes and other organic.

The characteristics of Acetamide,N-(2-nitrophenyl)- are as followings: (1)ACD/LogP: 1.00; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1; (4)ACD/LogD (pH 7.4): 1; (5)ACD/BCF (pH 5.5): 3.39; (6)ACD/BCF (pH 7.4): 3.39; (7)ACD/KOC (pH 5.5): 83.37; (8)ACD/KOC (pH 7.4): 83.37; (9)#H bond acceptors: 5; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 66.13 Å2; (13)Index of Refraction: 1.617; (14)Molar Refractivity: 47.07 cm3; (15)Molar Volume: 134.3 cm3; (16)Polarizability: 18.66×10-24cm3; (17)Surface Tension: 55.3 dyne/cm; (18)Density: 1.34 g/cm3; (19)Flash Point: 188.5 °C; (20)Enthalpy of Vaporization: 63.73 kJ/mol; (21)Boiling Point: 388.1 °C at 760 mmHg; (22)Vapour Pressure: 3.14E-06 mmHg at 25°C. 

Preparation of Acetamide,N-(2-nitrophenyl)-: This chemical can be prepared by acetic acid anhydride and 2-nitro-aniline. The reaction will need reagent Mg(ClO4)2. The reaction time is 0.5 hours with temperature of 20°C, and the yield is about 89%.

Uses of Acetamide,N-(2-nitrophenyl)-: It can react with 3-bromo-2-methyl-propene to produce o-nitro-N-(2-methyl-2-propenyl)acetanilide. This reaction will need reagent KOH, and the menstruum acetone. The reaction time is 3 minutes with heating, and the yield is about 92%.

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