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Hydrazinecarboxamide,2-(phenylmethylene)-

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Name

Hydrazinecarboxamide,2-(phenylmethylene)-

EINECS 216-397-0
CAS No. 1574-10-3 Density 1.19 g/cm3
PSA 67.48000 LogP 1.78000
Solubility N/A Melting Point 213.5-217.5 °C(lit.)
Formula C8H9N3O Boiling Point N/A
Molecular Weight 163.179 Flash Point N/A
Transport Information N/A Appearance N/A
Safety 22-24/25 Risk Codes N/A
Molecular Structure Molecular Structure of 1574-10-3 (BENZALDEHYDE SEMICARBAZONE  97) Hazard Symbols N/A
Synonyms

Benzaldehyde,semicarbazone (6CI,7CI,8CI);1-Benzylidenesemicarbazide;3-Hydroxybenzaldehydesemicarbazone;Benzylidenesemicarbazide;NSC 1591;(Benzylideneamino)urea;

Article Data 59

Hydrazinecarboxamide,2-(phenylmethylene)- Specification

The Hydrazinecarboxamide,2-(phenylmethylene)- with CAS registry number of 1574-10-3 is also known as 1-Benzylidenesemicarbazide. The IUPAC name is (Benzylideneamino)urea. It belongs to product categories of Hydrazones; Nitrogen Compounds; Organic Building Blocks. Its EINECS registry number is 216-397-0. In addition, the formula is C8H9N3O and the molecular weight is 163.18. This chemical should be stored in dark, dry and ventilated place. During using it, do not breathe dust and avoid contact with skin and eyes.

Physical properties about Hydrazinecarboxamide,2-(phenylmethylene)- are: (1)ACD/LogP: 1.27; (2)ACD/LogD (pH 5.5): 1.27; (3)ACD/LogD (pH 7.4): 1.27; (4)ACD/BCF (pH 5.5): 5.43; (5)ACD/BCF (pH 7.4): 5.43; (6)ACD/KOC (pH 5.5): 116.92; (7)ACD/KOC (pH 7.4): 116.9; (8)#H bond acceptors: 4; (9)#H bond donors: 3; (10)#Freely Rotating Bonds: 2; (11)Index of Refraction: 1.586; (12)Molar Refractivity: 45.73 cm3; (13)Molar Volume: 136.2 cm3; (14)Surface Tension: 49.1 dyne/cm; (15)Density: 1.19 g/cm3.

Preparation of Hydrazinecarboxamide,2-(phenylmethylene)-: it is prepared by reaction of benzaldehyde with semicarbazide; hydrochloride. The reaction needs reagent pyridine and solvents methanol, H2O. The yield is about 77%.

Hydrazinecarboxamide,2-(phenylmethylene)- is prepared by reaction of benzaldehyde with semicarbazide; hydrochloride.

Uses of Hydrazinecarboxamide,2-(phenylmethylene)-: it is used to produce 2-(4-chlorobenzyl)-1-benzylidenesemicarbazide by reaction with 1-chloro-4-chloromethyl-benzene. The reaction occurs with reagent sodium hydroxide and solvents ethanol, H2O with other condition of heating for 9 hours. The yield is about 84.3%.

Hydrazinecarboxamide,2-(phenylmethylene)- is used to produce 2-(4-chlorobenzyl)-1-benzylidenesemicarbazide by reaction with 1-chloro-4-chloromethyl-benzene.

You can still convert the following datas into molecular structure:
1. Canonical SMILES: C1=CC=C(C=C1)C=NNC(=O)N
2. InChI: InChI=1S/C8H9N3O/c9-8(12)11-10-6-7-4-2-1-3-5-7/h1-6H,(H3,9,11,12)
3. InChIKey: AKGUXECGGCUDCV-UHFFFAOYSA-N

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