3-FLUOROBENZHYDRAZIDE
3-FLUOROBENZHYDRAZIDE Basic information
- Product Name:
- 3-FLUOROBENZHYDRAZIDE
- Synonyms:
-
- 3-FLUOROBENZOIC ACID HYDRAZIDE
- 3-FLUOROBENZOIC HYDRAZIDE
- 3-FLUOROBENZOHYDRAZIDE
- 3-FLUOROBENZHYDRAZIDE
- 3-Fluorobenzhydrazide 98%
- 3-Fluorobenzhydrazide98%
- BUTTPARK 35\03-72
- 3-Fluorobenzoic hydrazide 97%
- CAS:
- 499-55-8
- MF:
- C7H7FN2O
- MW:
- 154.14
- Product Categories:
-
- Aryl Fluorinated Building Blocks
- Building Blocks
- C7-C8
- Carbonyl Compounds
- Chemical Synthesis
- Fluorinated Building Blocks
- Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
- Phenyls & Phenyl-Het
- Fluorine Compounds
- Phenyls & Phenyl-Het
- Carbonyl Compounds
- Organic Building Blocks
- Organic Fluorinated Building Blocks
- Other Fluorinated Organic Building Blocks
- Hydrazides
- Organic Building Blocks
- Mol File:
- 499-55-8.mol
3-FLUOROBENZHYDRAZIDE Chemical Properties
- Melting point:
- 139-143 °C (lit.)
- Density
- 1.272±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 11.78±0.10(Predicted)
- form
- Crystalline Powder
- color
- White to off-white
- CAS DataBase Reference
- 499-55-8(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 20/21/22-36/37/38
- Safety Statements
- 26-36/37/39-36
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 2928009090
3-FLUOROBENZHYDRAZIDE Usage And Synthesis
Uses
3-FLUOROBENZHYDRAZIDE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
Synthesis
Hydrazides (30-58) were synthesized by one pot conventionalmethod24 Benzoic acid or its derivative (10 mmol) was dissolvedin ethanol (20 mL). Sulfuric acid (3 N, 2 mL) was added and thereaction contents were refluxed for six hours. The reaction wasmonitored with TLC. After the completion of the reaction, the reactionmixture was neutralized by adding solid NaHCO3, and filteredto remove excess of NaHCO3. In the neutralized reaction mixture which contains ethyl ester, hydrazine monohydrate (1.5 mL,3 mmol) was added and refluxed for 3-6 h to complete the reaction.Ethanol and unreacted hydrazine were removed by distillationupto 1/3 volume. The reaction contents were cooled, filteredand recrystallized from methanol to obtain the desired hydrazidecrystals (see Supporting information).
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