2-Bromobutyric acid

Chemical compound 2-Bromobutyric acid 2-Bromobutyric acid.svg 150px 2-Bromobutyric acid-3D-balls-by-AHRLS-2012.png 150px 2-Bromobutyric acid-3D-vdW-by-AHRLS-2012.png 150px 2-Bromobutyric acid-3D-sticks-by-AHRLS-2012.png 150px 2-Bromobutanoic acid 2-Bromobutyric acidalpha-Bromobytyric aciddl-2-Bromobutyric acidα-Bromobutyricacid 80-58-0 racemic 2681-94-9 R enantiomer 32659-49-7 S enantiomer correct CAS correct FDA MCO6PW23BT 201-294-5 6655 CCC(Br)C(=O)O 6403 1/C4H7BrO2/c1-2-3(5)4(6)7/h3H,2H2,1H3,(H,6,7) YAQLSKVCTLCIIE-UHFFFAOYAL 1S/C4H7BrO2/c1-2-3(5)4(6)7/h3H,2H2,1H3,(H,6,7) YAQLSKVCTLCIIE-UHFFFAOYSA-N 4 7 1 2 colorless liquid 1.567 g/mL at 25 °C −4 racemate 99 to 103 10 mmHg 66 g/L (20 °C) 0.0533 Torr 2.95±0.10. Most Acidic Temp: 25 °C Causes severe skin burns and eye damage. Causes serious eye damage. Harmful if swallowed. 05 07 Danger 302 314 260 264 270 280 301+312 301+330+331 303+361+353 304+340 305+351+338 310 321 330 363 405 501 > 112 2-Bromobutyride 2-Bromobutyric acid is the organic compound with the molecular formula CH3CH2CH(Br)CO2H. It is a colorless liquid. The 2-position is stereogenic, so the compound is chiral. Optical resolution can be effected using strychnine.10.1002/prac.19321351103 Über die α-Brom-n-buttersäure. (II. Mitteilung). Die Zerlegung der racem-Säure 1932 Ahlberg R. Journal für Praktische Chemie 135 11–12 335–344 2-Bromobutyric acid is used as a building block chemical, such as in the preparation of Levetiracetam,November 2012 an anticonvulsant medication.https://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001067/ Levetiracetam - PubMed Health 2017-11-01 2012-11-30 https://web.archive.org/web/20121130095529/http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001067/ dead Production (±)-2-Bromobuyric acid may be prepared by the acid-catalyzed Hell–Volhard–Zelinsky reaction, where butyric acid is treated with elemental bromine. It is one of many compounds that arise adventiously from the use of bromine as an antiseptic.10.1021/es060353j Occurrence of a New Generation of Disinfection Byproducts 2006 Krasner Stuart W. Weinberg Howard S. Richardson Susan D. Pastor Salvador J. Chinn Russell Sclimenti Michael J. Onstad Gretchen D. Thruston Alfred D. Environmental Science & Technology 40 23 7175–7185 17180964 400px References Category:Carboxylic acids Category:Organobromides