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Benzamide, N-p-tolyl-

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Name

Benzamide, N-p-tolyl-

EINECS 209-491-8
CAS No. 582-78-5 Density 1.144 g/cm3
PSA 29.10000 LogP 3.32030
Solubility N/A Melting Point 158 °C
Formula C14H13NO Boiling Point 265.3 °C at 760 mmHg
Molecular Weight 211.263 Flash Point 154.9 °C
Transport Information N/A Appearance N/A
Safety Risk Codes N/A
Molecular Structure Molecular Structure of 582-78-5 (4'-methylbenzanilide) Hazard Symbols N/A
Synonyms

p-Toluoylaniline;N-Benzoyl-p-toluidine;Benzoic acid p-toluidide;Benzamide, N-(4-methylphenyl)-;Benzamide, N- (4-methylphenyl)-;p-Benzotoluidide;N-(4-methylphenyl)benzamide;4'-Methylbenzanilide;

Article Data 353

Benzamide, N-p-tolyl- Specification

The Benzamide, N-p-tolyl-, with the CAS registry number 582-78-5, is also known as 4'-Methylbenzanilide. Its EINECS number is 209-491-8. This chemical's molecular formula is C14H13NO and molecular weight is 211.26. What's more, its IUPAC name is N-(4-methylphenyl)benzamide.

Physical properties of Benzamide, N-p-tolyl- are: (1)ACD/LogP: 3.36; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3; (4)ACD/LogD (pH 7.4): 3; (5)ACD/BCF (pH 5.5): 209; (6)ACD/BCF (pH 7.4): 209; (7)ACD/KOC (pH 5.5): 1593; (8)ACD/KOC (pH 7.4): 1593; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 29.1 Å2; (13)Index of Refraction: 1.63 ; (14)Molar Refractivity: 65.653 cm3; (15)Molar Volume: 184.58 cm3; (16)Polarizability: 26.027×10-24cm3; (17)Surface Tension: 47.489 dyne/cm; (18)Density: 1.145 g/cm3; (19)Flash Point: 155.727 °C; (20)Enthalpy of Vaporization: 50.454 kJ/mol; (21)Boiling Point: 266.559 °C at 760 mmHg; (22)Vapour Pressure: 0.009 mmHg at 25°C.

Preparation of Benzamide, N-p-tolyl-: this chemical can be prepared by 4-methyl-aniline, benzoic acid hydrazide. This reaction will need reagent HgO and solvent benzene with the reaction time of 30 min. The yield is about 87%.

Benzamide, N-p-tolyl- can be prepared by 4-methyl-aniline, benzoic acid hydrazide.

Uses of Benzamide, N-p-tolyl-: it can be used to produce N-benzyl-p-toluidine by heating. It will need reagents lithium aluminum hydride and solvent tetrahydrofuran with the reaction time of 2 hours. The yield is about 76%.

Benzamide, N-p-tolyl- can be used to produce N-benzyl-p-toluidine by heating.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CC1=CC=C(C=C1)NC(=O)C2=CC=CC=C2
(2)InChI: InChI=1S/C14H13NO/c1-11-7-9-13(10-8-11)15-14(16)12-5-3-2-4-6-12/h2-10H,1H3,(H,15,16)
(3)InChIKey: YUIHXKGKVSVIEL-UHFFFAOYSA-N

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