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About This Item
Empirical Formula (Hill Notation):
C7H7N3O
CAS Number:
Molecular Weight:
149.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
98%
Quality Segment
assay
98%
reaction suitability
reaction type: C-C Bond Formation
mp
150-152 °C (lit.)
functional group
hydroxyl
SMILES string
OCn1nnc2ccccc12
InChI
1S/C7H7N3O/c11-5-10-7-4-2-1-3-6(7)8-9-10/h1-4,11H,5H2
InChI key
MXJIHEXYGRXHGP-UHFFFAOYSA-N
Application
Safe reagent for the in situ generation of anhydrous formaldehyde in organic solvents.
Catalyst for:
Used as:
Reactant for:
- Hydrolysis of phenyl esters of a-furoic acid
Used as:
- Corrosion inhibitor of iron in aerated acidic media
- Reactive oxygen scavenger
Reactant for:
- Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation
- Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement
- Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors
- Gosteli-Claisen rearrangement
signalword
Warning
hcodes
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
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