| Weight | 107.54 g/mol |
|---|---|
| Formula | C3H6ClNO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
3-Chloropropionamide (5875-24-1)
chloropropionamide
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- Lewis Acid Mediated Aminolysis of Esters: Conversion of Methyl (S)-(-)-2-Chloropropionate to (S)-(+)-N, N-Diethyl-2-chloropropionamide (Synthetic Communications, 1986)
- Chichibabin Reaction. III. Chichibabin Reaction of 7-Methylquinoline and Migration of the Methyl Group in Friedel-Crafts Reaction of N-(m-Tolyl)- and N-(p-Tolyl)--chloropropionamide (Studies on the Syntheses of Heterocyclic Compounds. CCXV) (Chemical & Pharmaceutical Bulletin, 1968)
- X-Ray Structure of a Reaction Intermediate of L-2-Haloacid Dehalogenase with L-2-Chloropropionamide (Journal of Biochemistry, 1998)
- N-BENZYL--CHLOROPROPIONAMIDE (HIBICON): A New Approach to Anticonvulsant Therapy (Journal of Nervous and Mental Disease, 1952)
- THE PHARMACOLOGY OF N-BENZYL--CHLOROPROPIONAMIDE (HIBICON), A NEW ANTICONVULSANT (Journal of Pharmacology and Experimental Therapeutics, 1953)
- Synthesis of N4-(2-acetamido-2-deoxy--d-glucopyranosyl)-l-asparagine analogues. n-Butyramide, 3-chloropropionamide, 3-aminopropionamide, and isovaleramide analogues (Carbohydrate Research, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - chloropropionamide
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SMILESC(CCl)C(=O)N
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InChIKeyJQDXZJYAUSVHDH-UHFFFAOYSA-N
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