| Weight | 133.15 g/mol |
|---|---|
| Formula | C8H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Mandelonitrile (532-28-5)
mandelonitrile, (+-)-isomer
Score:
#1581 in Biochemistry
,
#3626 in Biology
,
#4552 in Chemistry
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- Sigma-Aldrich - Search for Mandelonitrile
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- TCI - Mandelonitrile55.00 USD
- Production of R-(-)-mandelic acid from mandelonitrile by Alcaligenes faecalis ATCC 8750. (Applied and Environmental Microbiology, 1991)
- Purification and characterization of the nitrilase from Alcaligenes faecalis ATCC 8750 responsible for enantioselective hydrolysis of mandelonitrile (Journal of Fermentation and Bioengineering, 1992)
- Screening for enantioselective nitrilases : Kinetic resolution of racemic mandelonitrile to (R)-(-)-mandelic acid by new bacterial isolates (Tetrahedron-asymmetry, 2004)
- Temporal and Spatial Expression of Amygdalin Hydrolase and (R)-(+)-Mandelonitrile Lyase in Black Cherry Seeds (Plant Physiology, 1995)
- Benzoyl cyanide and mandelonitrile benzoate in the defensive secretions of millipedes (Journal of Chemical Ecology, 1977)
- Formation of C-C bonds by mandelonitrile lyase in organic solvents (Biotechnology and Bioengineering, 1990)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - mandelonitrile, (+-)-isomer
-
SMILESC1=CC=C(C=C1)C(C#N)O
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InChIKeyNNICRUQPODTGRU-UHFFFAOYSA-N
- Pubchem - Mandelonitrile
- Wikipedia - mandelonitrile
In organic chemistry, mandelonitrile is the cyanohydrin derivative of benzaldehyde. Small amounts of mandelonitrile occur in the pits of some fruits.
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