Skip to Content
Merck
CN

151653

Methyl hydrazinocarboxylate

97%

Synonym(s):

Methoxycarbonylhydrazine, Methyl carbazate

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
H2NNHCO2CH3
CAS Number:
Molecular Weight:
90.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-560-3
MDL number:
Assay:
97%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

assay

97%

bp

108 °C/12 mmHg (lit.)

mp

70-73 °C (lit.)

functional group

amine, hydrazine

SMILES string

COC(=O)NN

InChI

1S/C2H6N2O2/c1-6-2(5)4-3/h3H2,1H3,(H,4,5)

InChI key

WFJRIDQGVSJLLH-UHFFFAOYSA-N

Application

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.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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
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



Global Trade Item Number

SKUGTIN
151653-100G04061838739339
151653-500G04061832491523