L-Phenylalanine hydrazide
(S)-2-amino-3-phenylpropanehydrazide
CAS: 52386-52-4
Molecular Formula: C9H13N3O
L-Phenylalanine hydrazide - Names and Identifiers
| Name | (S)-2-amino-3-phenylpropanehydrazide |
| Synonyms | H-Phe-NHNH2 H-PHE-NHNH2 L-PHENYLALANINE HYDRAZIDE L-Phenylalanine hydrazide 2-amino-3-phenylpropanehydrazide (S)-2-amino-3-phenylpropanehydrazide (2S)-2-amino-3-phenylpropanehydrazide |
| CAS | 52386-52-4 |
| InChI | InChI=1/C9H13N3O/c10-8(9(13)12-11)6-7-4-2-1-3-5-7/h1-5,8H,6,10-11H2,(H,12,13) |
L-Phenylalanine hydrazide - Physico-chemical Properties
| Molecular Formula | C9H13N3O |
| Molar Mass | 179.22 |
| Density | 1.175±0.06 g/cm3(Predicted) |
| Boling Point | 410.0±38.0 °C(Predicted) |
| Flash Point | 201.7°C |
| Vapor Presure | 6.25E-07mmHg at 25°C |
| pKa | 12.86±0.50(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.585 |
L-Phenylalanine hydrazide - Introduction
(S)-I (S)-I) is an organic compound whose chemical formula is C9H13N3O. It is a white crystalline powder, soluble in water and some organic solvents.
(S)-It is mainly used as a catalytic reducing agent in pharmaceutical synthesis and organic synthesis. It plays an important role in the preparation of drugs and pesticides, and can be used as synthetic hormone drugs and enzyme inhibitors.
The synthesis method of (S)-is usually obtained by a substitution reaction of L-phenylalanine. Substituents can be selected from chlorinated alkanes or other substituted compounds, which react with ammonia and hydrogen hydrazine to form (S)-phenyl.
When using (S)-ceramic, you need to pay attention to its safety. It is a toxic chemical and should follow laboratory safety requirements. Contact with the skin or inhalation of the compound may cause irritation or injury. Should be sealed to avoid contact with oxidizing agents.
(S)-It is mainly used as a catalytic reducing agent in pharmaceutical synthesis and organic synthesis. It plays an important role in the preparation of drugs and pesticides, and can be used as synthetic hormone drugs and enzyme inhibitors.
The synthesis method of (S)-is usually obtained by a substitution reaction of L-phenylalanine. Substituents can be selected from chlorinated alkanes or other substituted compounds, which react with ammonia and hydrogen hydrazine to form (S)-phenyl.
When using (S)-ceramic, you need to pay attention to its safety. It is a toxic chemical and should follow laboratory safety requirements. Contact with the skin or inhalation of the compound may cause irritation or injury. Should be sealed to avoid contact with oxidizing agents.
Last Update：2024-04-09 19:05:50
