151653
Methylhydrazinocarboxylat
97%
Synonym(e):
Carbazidsäuremethylester, Methoxycarbonylhydrazin
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Alle Fotos(3)
About This Item
Lineare Formel:
H2NNHCO2CH3
CAS-Nummer:
Molekulargewicht:
90.08
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
97%
bp
108 °C/12 mmHg (lit.)
mp (Schmelzpunkt)
70-73 °C (lit.)
Funktionelle Gruppe
amine
hydrazine
SMILES String
COC(=O)NN
InChI
1S/C2H6N2O2/c1-6-2(5)4-3/h3H2,1H3,(H,4,5)
InChIKey
WFJRIDQGVSJLLH-UHFFFAOYSA-N
Anwendung
Methyl hydrazinocarboxylate (Methyl carbazate) was used in the preparation of methyl 3-(4-methyl-benzyl-idene)carbazate. It was also used in the synthesis of imidazo[1,5-d][1,2,4]triazines.
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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Yu-Feng Li et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 6), o1429-o1429 (2010-01-01)
The title compound, C(10)H(12)N(2)O(2), was prepared by the reaction of methyl carbazate and 4-methyl-benzaldehyde. The dihedral angle between the benzene ring and the carbazate fragment is 20.86 (10)°. In the crystal structure, mol-ecules are linked by inter-molecular N-H⋯O hydrogen bonds.
R Truhaut et al.
Toxicology, 22(3), 219-221 (1981-01-01)
Methyl carbazate, a metabolite of carbadox in the rat, was administered orally to rats for 2 years. The compound was mixed in the diet at concentrations corresponding to dose levels of 0, 2.5, 5 and 10 mg/kg body wt/day. There
R Paul et al.
Journal of medicinal chemistry, 28(11), 1704-1716 (1985-11-01)
By using inhibition of histamine release from antigen-challenged, sensitized human basophils as a means of identifying a potentially prophylactic drug for the treatment of asthma, a series of substituted imidazo[1,5-d][1,2,4]triazines were found, which were active. These compounds were prepared by
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