Identification | More | [Name]
INDOLE-3-ACETIC ACID HYDRAZIDE | [CAS]
5448-47-5 | [Synonyms]
INDOLE 3-ACETHYDRAZIDE INDOLE-3-ACETIC ACID HYDRAZIDE INDOLE-3-ACETIC HYDRAZIDE TIMTEC-BB SBB003669 1-(3-indolylacetyl)-hydrazin 1-(3-Indolylacetyl)hydrazine 1H-Indole-3-acetic acid, hydrazide 2-(1H-Indol-3-yl)acetohydrazide 3-Indolylacetic acid hydrazide Hydrazine, 1-(3-indolylacetyl)- 3-indoleacetic acid hydrazide Indol-3-ylacetic acid hydrazide Indole-3-aceticacidhydrazide,98% Indole-3-acetic acid hyrazide (1H-Indole-3-yl)acetohydrazide 1H-Indole-3-acetohydrazide 1H-Indole-3-ylacetic acid hydrazide | [EINECS(EC#)]
226-672-7 | [Molecular Formula]
C10H11N3O | [MDL Number]
MFCD00005634 | [Molecular Weight]
189.21 | [MOL File]
5448-47-5.mol |
Chemical Properties | Back Directory | [Appearance]
beige to pale brown fine crystalline powder | [Melting point ]
142-145 °C (lit.) | [Boiling point ]
324.47°C (rough estimate) | [density ]
1.1654 (rough estimate) | [refractive index ]
1.4830 (estimate) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [pka]
13.23±0.18(Predicted) | [CAS DataBase Reference]
5448-47-5(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
22-36/37/38 | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
NL3600000
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT |
Hazard Information | Back Directory | [Chemical Properties]
beige to pale brown fine crystalline powder | [Uses]
Reactant for preparation of:
- Antifungal agents
- Anticonvulsant agents
- Alpha-4 (α4) integrin antagonists
- A fluorescent analogue of UDP-N-acetylglucosamine
- Antioxidant agents with myocardial protection properties
- Antagonist agents of neuropeptide Y receptors
- Antibacterial agents
- Potential monoamine oxidase inhibitors
| [Uses]
Reactant for preparation of:• ;Antifungal agents1• ;Anticonvulsant agents2• ;Alpha-4 (α4) integrin antagonists3• ;A fluorescent analogue of UDP-N-acetylglucosamine4• ;Antioxidant agents with myocardial protection properties5• ;Antagonist agents of neuropeptide Y receptors6• ;Antibacterial agents7• ;Potential monoamine oxidase inhibitors8 |
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