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3-FLUOROBENZHYDRAZIDE

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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
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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)
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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
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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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