2-PHENYL-ACETAMIDINE
- CAS NO.：5504-24-5
- Empirical Formula: C8H10N2
- Molecular Weight: 134.18
- MDL number: MFCD01108399
- SAFETY DATA SHEET (SDS)
- Update Date: 2022-08-26 12:23:39
What is 2-PHENYL-ACETAMIDINE?
The Uses of 2-PHENYL-ACETAMIDINE
2-Phenylacetamidine is a useful synthetic intermediate. It is used in the synthesis of non-nucleoside reverse transcriptase inhibitors. It is also used to prepare naltrexone-derived pyrido- and pyrimidomorphinans.
Properties of 2-PHENYL-ACETAMIDINE
| Melting point: | 62-63 °C |
| Boiling point: | 243.1±33.0 °C(Predicted) |
| Density | 1.06 |
| storage temp. | 2-8°C(protect from light) |
| pka | 12.62±0.40(Predicted) |
Safety information for 2-PHENYL-ACETAMIDINE
| Signal word | Warning |
| Pictogram(s) |
 Exclamation Mark Irritant GHS07 |
| GHS Hazard Statements |
H302:Acute toxicity,oral H319:Serious eye damage/eye irritation |
| Precautionary Statement Codes |
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
Computed Descriptors for 2-PHENYL-ACETAMIDINE
New Products
4,4-Difluoropiperidine hydrochloride tert-butyl 9-methoxy-3-azaspiro[5.5]undecane-3-carboxylate Indole Methyl Resin N-Isopropylurea N,N-Dicyclohexylcarbodiimide(DCC) MELDRUMS ACID 5-METHYLISOXAZOLE-4-CARBOXYLIC ACID Magnessium Bis glycinate Zinc ascorbate 1-bromo-2-butyne 2-acetamidophenol 9(10H)-anthracenone Erythrosin B, 4-Piperidinopiperidine 2-((4-morpholinophenylamino) (methylthio) methylene) malononitrile 2,4-dihydroxybenzaldehyde 3-(4-morpholinophenylamino)-5-amino-1H-pyrazole-4-carbonitrile Methyl 2-methylquinoline-6-carboxylate 2,6-dichloro-4-nitropyridine 4-Bromo-2-chlorobenzonitrile 2-(benzylamino)acetic acid hydrochloride 4-(tert-Butoxycarbonylamino)but- 2-ynoic acid 3,4-dihydro-2H-benzo[b][1,4]dioxepine 1-Phenyl-1-cycloprppanecarboxylicacidRelated products of tetrahydrofuran
![ETHYL 2-(([1-AMINO-2-(4-NITROPHENYL)ETHYLIDENE]AMINO)OXY)-2-OXOACETATE](https://img.chemicalbook.in/StructureFile/ChemBookStructure2/GIF/CB9350616.gif)
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