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Acetic hydrazide, 96%, Thermo Scientific Chemicals
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Catalog number A10969.36
also known as A10969-36
Price (USD)/ Each
575.00
-
Quantity:
500 g
Price (USD)/ Each
575.00
Acetic hydrazide, 96%, Thermo Scientific Chemicals
Catalog numberA10969.36
Price (USD)/ Each
575.00
-
Chemical Identifiers
CAS1068-57-1
IUPAC Nameacetohydrazide
Molecular FormulaC2H6N2O
InChI KeyOFLXLNCGODUUOT-UHFFFAOYSA-N
SMILESCC(=O)NN
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Translucent colorless or white
FormCrystals or crystalline powder or powder or chunks/lumps
Assay (unspecified)≥95.0%
CommentSpecification differs for U.S. and non-U.S. material where indicated
Identification (FTIR)Conforms (non-U.S. specification)
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Acetic hydrazide is used as an antibiotic for the treatment of mycobacterium tuberculosis. It is also involved in the preparation of sunitinib b reacting with 5-fluoroisatin. Further, it inhibits mycolic acid biosynthesis. It serves as an important intermediate in organic synthesis such as nitric furosemide Long (nifuratrone) in medicine.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Acetic hydrazide is used as an antibiotic for the treatment of mycobacterium tuberculosis. It is also involved in the preparation of sunitinib b reacting with 5-fluoroisatin. Further, it inhibits mycolic acid biosynthesis. It serves as an important intermediate in organic synthesis such as nitric furosemide Long (nifuratrone) in medicine.
Solubility
Soluble in water.
Notes
Hygroscopic. Incompatible with strong bases.
Acetic hydrazide is used as an antibiotic for the treatment of mycobacterium tuberculosis. It is also involved in the preparation of sunitinib b reacting with 5-fluoroisatin. Further, it inhibits mycolic acid biosynthesis. It serves as an important intermediate in organic synthesis such as nitric furosemide Long (nifuratrone) in medicine.
Solubility
Soluble in water.
Notes
Hygroscopic. Incompatible with strong bases.
RUO – Research Use Only
General References:
- Sadhukhan, D.; Maiti, M.; Pilet, G.; Bauzá, A.; Frontera, A.; Mitra, S. Hydrogen Bond, pi-pi, and CH-pi Interactions Governing the Supramolecular Assembly of Some Hydrazone Ligands and Their MnII Complexes - Structural and Theoretical Interpretation. Eur. J. Inorg. Chem. 2015, 2015 (11), 1958-1972.
- Sadhukhan, D.; Maiti, M.; Zangrando, E.; Pathan, S.; Mitra, S.; Patel, A. Heterogeneous catalytic oxidation of styrene by an oxo bridged divanadium(V) complex of an acetohydrazide-Schiff base. Polyhedron 2014, 69, 1-9.