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CAS RN: 624-84-0 | Product Number: F0667

Formohydrazide


Purity: >97.0%(HPLC)
Synonyms:
  • Formic Hydrazide
  • Formic Acid Hydrazide
Product Documents:
25G
$61.00
1   1   ≥100 
100G
$167.00
1   Contact Us 24  

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Product Number F0667
Purity / Analysis Method >97.0%(HPLC)
Molecular Formula / Molecular Weight CH__4N__2O = 60.06 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Hygroscopic,Heat Sensitive
CAS RN 624-84-0
Reaxys Registry Number 635759
PubChem Substance ID 354334127
MDL Number

MFCD00007589

Specifications
Appearance White to Almost white powder to crystal
Purity(HPLC) min. 97.0 area%
Purity(Nonaqueous Titration) min. 95.0 %
Melting point 56.0 to 61.0 °C
Properties (reference)
Melting Point 59 °C
Boiling Point 90 °C/0.7 mmHg
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P302 + P352 : IF ON SKIN: Wash with plenty of soap and water.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
P362 : Take off contaminated clothing and wash before reuse.
Related Laws:
RTECS# LQ8615000
Transport Information:
HS Number 2928.00.5000
Application
Hydrazide Useful for Construction of Heterocycles

Experimental procedure: 1,3-Diphenyl thiourea (0.5 g, 2.19 mmol) is added to a stirred solution of IBX (0.65 g, 2.19 mmol) and triethylamine (1 mL, 7.11 mmol) in DMF (10 mL) for 5 min. Then, formohydrazide (0.45 g, 7.04 mmol) is slowly added to the reaction mixture with continued stirring for 3 h at rt. After completion, the reaction mixture is poured into a saturated solution of NaHCO3 (20 mL). The aqueous layer is extracted with ethyl acetate (3 × 15 mL). The combined organic layers are dried over Na2SO4 and evaporated to afford the crude product, which is purified by column chromatography on silica gel (petroleum ether : ethyl acetate) to afford 0.37 g of 1 as a white solid in 72% yield.

References


PubMed Literature


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