| Weight | 134.134 g/mol |
|---|---|
| Formula | C8H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
phenylglyoxal (1074-12-0)
Score:
#2105 in Biochemistry
,
#4353 in Biology
,
#5492 in Chemistry
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- The Reaction of Phenylglyoxal with Arginine Residues in Proteins (Journal of Biological Chemistry, 1968)
- Further studies on the reactions of phenylglyoxal and related reagents with proteins (Journal of Biochemistry, 1977)
- The reactions of phenylglyoxal and related reagents with amino acids. (Journal of Biochemistry, 1977)
- Irreversible inactivation of red cell chloride exchange with phenylglyoxal, and arginine-specific reagent. (The Journal of General Physiology, 1982)
- Reaction of phenylglyoxal with arginine. The effect of buffers and pH (Biochemical and Biophysical Research Communications, 1979)
- A comparison of the effects of cyanide, hydrogen peroxide, and phenylglyoxal on eucaryotic and procaryotic Cu,Zn superoxide dismutases (Archives of Biochemistry and Biophysics, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=O)C=O
-
InChIKeyOJUGVDODNPJEEC-UHFFFAOYSA-N
- Pubchem - phenylglyoxal
- Wikipedia - phenylglyoxal
Phenylglyoxal is the organic compound with the formula C6H5C(O)C(O)H. It contains both an aldehyde and a ketone functional group. It is yellow liquid when anhydrous but readily forms a colorless crystalline hydrate.
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phenylglyoxal
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