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About This Item
Empirical Formula (Hill Notation):
C9H12N2O3
CAS Number:
Molecular Weight:
196.20
Beilstein:
2052164
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
≥98.0%
mp
75-78 °C
SMILES string
COc1ccc(COC(=O)NN)cc1
InChI
1S/C9H12N2O3/c1-13-8-4-2-7(3-5-8)6-14-9(12)11-10/h2-5H,6,10H2,1H3,(H,11,12)
InChI key
JKBMMHKEAGEILO-UHFFFAOYSA-N
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Application
4-Methoxybenzyl carbazate may be used to synthesize 5,10-diiminoporphodimethene (a dearomatized porphyrinoid) and N-(2,4-dihydroxythiobenzoyl)-4-methoxybenzyl carbazate
Other Notes
Starting material for the azide used to introduce the pMZ-amino protection which is removable under mild hydrolytic conditions
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Synthesis and fungistatic activity of new groups of 2, 4-dihydroxythiobenzoyl derivatives against phytopathogenic fungi
Legocki, Jan, et al.
Journal of Agricultural and Food Chemistry, 51.2 , 362-368 (2003)
H. Yamada et al.
Bulletin of the Chemical Society of Japan, 57, 3333-3333 (1984)
Experimental and Theoretical Characterization of 5, 10-Diminoporphodimethenes: Dearomatized Porphyrinoids from Palladium-Catalyzed Hydrazinations of 5, 10-Diarylporphyrins.
Basic B, et al.
ChemPlusChem, 79(6), 813-824 (2014)
C. Ressler et al.
The Journal of Organic Chemistry, 36, 3961-3961 (1971)
F. Weygand et al.
Chemische Berichte, 95, 1-1 (1962)
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