1,2-dibromoethane

COc1ccc([CH2][Mg][Br])cc1
Reaction #1846
Anisylmagnesium Bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)([O-])CCS(=O)(=O)[O-].[Na+].[Na+]
Reaction #2026
title compound
Yield 65.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNN=NCCN=NNC
Reaction #2786
off-white solid
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)NC(=O)c2cc(OCCBr)ccc2O1
Reaction #4622
6-(2-Bromoethoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1(C)NC(=O)c2ccc(OCCBr)cc2O1
Reaction #4635
2,3-dihydro-2,2-dimethyl-7-(2-bromoethoxy)-4H-1,3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NC(=O)c1c(O)cccc1OCCBr
Reaction #4636
6-(2-Bromoethoxy)salicylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1cccc(C(O)(C(F)(F)F)C(F)(F)F)c1
Reaction #4845
1-methoxy-3-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=S(=O)(c1cccc2cnccc12)N1CCN(CC=Cc2ccc(Cl)cc2)CC1
Reaction #5838
title compound
Yield 25.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(CC(=O)Nc2cccc(I)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7153
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(CC(=O)Nc2cccc(C3CCC(C(C)(C)C)CC3)c2)ccc1OCCBr
Reaction #7154
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(-c2nc3ccccc3o2)ccc1Cc1ccccn1
Reaction #7846
2-[3-methoxy-4-(pyridin-2-ylmethyl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(CC(=O)c2cccc(C)n2)cc1
Reaction #8321
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1cccc(CNCCBr)c1
Reaction #8732
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(CBr)c(C#N)c1
Reaction #9019
nitrile
Yield 44.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCc1cc2c(OC)ccc(Br)n2n1
Reaction #9285
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NC(=O)OCc1ccccc1
Reaction #10286
carbamic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cc(F)c2c(c1)OCCO2
Reaction #43586
desired compound
Yield 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc(Br)c2c(c1)OCCO2
Reaction #43602
desired compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1ccc2c(c1)OCCO2
Reaction #46213
2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester
Yield 29.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc(N(CCBr)n2cnnc2)cc1
Reaction #48177
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Page 1Next