Molecular Formula: C4H7Br
Molecular weight: 135.00238
InChi: InChI=1S/C4H7Br/c5-3-4-1-2-4/h4H,1-3H2
InChi Key: AEILLAXRDHDKDY-UHFFFAOYSA-N
SMILES: C1(CC1)CBr
Chemical Name
(bromomethyl)-cyclopropan
(bromomethyl)-cyclopropane
2-(bromomethyl)cyclopropane
bromomethyl-cyclopropane
cyclopropanemethyl bromide
cyclopropyl methyl bromide
methylcyclopropane bromide
(bromomethyl)-cyclopropan
(bromomethyl)-cyclopropane
2-(bromomethyl)cyclopropane
bromomethyl-cyclopropane
cyclopropanemethyl bromide
cyclopropyl methyl bromide
methylcyclopropane bromide
Authors of compound
Machara, Ales
Werner, Lukas
Hudlicky, Tomas
Adams, David R.
Cox, D. Phillip
Endoma-Arias, Mary Ann
Wernerova, Martina
Duchek, Jan
CARROLL, Robert
LEISCH, Hannes
Smrcina, Martin
PEDGRIFT, Brian
RAMOS, Antonio D.
THORPE, David S.
WIRE, William
ROSSE, Gerard
ZHAO, Jianhong
CLEMENS, Jennifer
LE, Tieu-Binh
JOHN, Stanly
FREED, Brian S.
FRANCIS, Robert S.
CAULFIELD, Thomas, J.
Werner, Lukas
Hudlicky, Tomas
Adams, David R.
Cox, D. Phillip
Endoma-Arias, Mary Ann
Wernerova, Martina
Duchek, Jan
CARROLL, Robert
LEISCH, Hannes
Smrcina, Martin
PEDGRIFT, Brian
RAMOS, Antonio D.
THORPE, David S.
WIRE, William
ROSSE, Gerard
ZHAO, Jianhong
CLEMENS, Jennifer
LE, Tieu-Binh
JOHN, Stanly
FREED, Brian S.
FRANCIS, Robert S.
CAULFIELD, Thomas, J.
Articles
Machara, Ales;
Werner, Lukas;
Hudlicky, Tomas;
Adams, David R.;
Cox, D. Phillip, Synthesis of buprenorphine from oripavine via N-demethylation of oripavine quaternary salts. Journal of Organic Chemistry 2011, 76(11), 4628 - 4634, 10.1021/jo200567n 
.
.
Machara, Ales;
Werner, Lukas;
Hudlicky, Tomas;
Cox, D. Phillip;
Endoma-Arias, Mary Ann, Improved synthesis of buprenorphine from thebaine and/or oripavine via palladium-catalyzed N-demethylation/acylation and/or concomitant O-demethylation. Advanced Synthesis and Catalysis 2012, 354(4), 613 - 626, 10.1002/adsc.201100807 .
.
Machara, Ales;
Werner, Lukas;
Hudlicky, Tomas;
Adams, David R.;
Cox, D. Phillip;
Endoma-Arias, Mary Ann;
Wernerova, Martina;
Duchek, Jan, Unexpected N-demethylation of oxymorphone and oxycodone N-oxides mediated by the burgess reagent: Direct synthesis of naltrexone, naloxone, and other antagonists from oxymorphone. Advanced Synthesis and Catalysis 2012, 354(14-15), 2706 - 2712, 10.1002/adsc.201200676 .
.
Patents
Machara, Ales;
Werner, Lukas;
Hudlicky, Tomas;
Adams, David R.;
CARROLL, Robert;
LEISCH, Hannes, PROCESSES FOR THE PREPARATION OF MORPHINANE AND MORPHINONE COMPOUNDS, WO2010/121369, 2010.
Machara, Ales;
Werner, Lukas;
Hudlicky, Tomas;
Endoma-Arias, Mary Ann;
Wernerova, Martina, Processes and Intermediates in the Preparation of Morphine Analogs via N-Demethylation of N-Oxides Using Cyclodehydration Reagents, US2012/283443, 2012.
Smrcina, Martin;
PEDGRIFT, Brian;
RAMOS, Antonio D.;
THORPE, David S.;
WIRE, William;
ROSSE, Gerard;
ZHAO, Jianhong;
CLEMENS, Jennifer;
LE, Tieu-Binh;
JOHN, Stanly;
FREED, Brian S.;
FRANCIS, Robert S.;
CAULFIELD, Thomas, J., SUBSTITUTED BENZOYLAMINO-INDAN-2-CARBOXYLIC ACIDS AND RELATED COMPOUNDS, WO2008/151211, 2008.