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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:
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* The storage conditions are subject to change without notice.
* The storage conditions are subject to change without notice.
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 | |
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. P302 + P352 : IF ON SKIN: Wash with plenty of water. 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. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
RTECS# | LQ8615000 |
Transport Information:
H.S.code* | 2928.00-000 |
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
- o-Iodoxybenzoic Acid Mediated Oxidative Desulfurization Initiated Domino Reactions for Synthesis of Azoles
PubMed Literature
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