Substructure Search

OC(CCl)c1ccccc1

COC(=O)/C(Cl)=C/c1ccc(OC)cc1
Reaction #4829
z-methyl-2-chloro-3-(4'-methoxyphenyl)propenoate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(Cl)=C/c1ccc(Cl)cc1
Reaction #4830
z-methyl-2-chloro-3-(4'-chlorophenyl)propenoate
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCC(O)c1ccc2c(c1)OCO2.Cl
Reaction #54278
1 -(3,4-methylenedioxyphenyl)-2-isopropylaminoethanol hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCNCC(O)c1ccc2c(c1)OCO2.Cl
Reaction #54280
1-(3,4-methylenedioxyphenyl)-2-ethylaminoethanol hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
OC(Cn1ccnc1)c1ccc(Cl)cc1Cl
Reaction #55723
desired product
Yield 66.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc([C@@H]2CO2)ccc1OCc1ccccc1
Reaction #58712
(R)-2-(4-Benzyloxy-3-nitrophenyl)oxirane
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2CCC1c1ccccc1
Reaction #65018
title compound
Yield 187.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C(O)CCl
Reaction #94597
α-chloromethyl-2-methoxybenzylalcohol
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCNCC(O)c2ccccc2OC)cc1OC.Cl
Reaction #94598
α-(3,4-dimethoxyphenethylaminomethyl)-2-methoxybenzylalcohol hydrochloride
Yield 41.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C(O)CCl
Reaction #94599
α-chloromethyl-2-methoxybenzylalcohol
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1CO1
Reaction #94600
2-(2-methoxyphenyl)oxirane
Yield 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(O)(Cn1ccnc1)c1ccc(Cl)cc1Cl
Reaction #175082
DOI: 10.1039/C8SC04228D
O=C(OCC(Cl)(Cl)Cl)c1ccc2c(c1)C(C(Cl)(Cl)Cl)OC(C(Cl)(Cl)Cl)O2
Reaction #178171
DOI: 10.1039/C8SC04228D
O=c1[nH]c2c(Cl)cc(C(O)CCl)cc2o1
Reaction #180875
DOI: 10.1039/C8SC04228D
O=C(O)C=CC(=O)O
Reaction #182639
DOI: 10.1039/C8SC04228D
CCCCC(O)(CCl)c1ccc(Cl)cc1Cl
Reaction #186186
DOI: 10.1039/C8SC04228D
OC(CCl)c1ccc(Cl)cc1Cl
Reaction #187066
DOI: 10.1039/C8SC04228D
OC(CCl)c1c(F)c(F)c(F)c(F)c1F
Reaction #195066
DOI: 10.1039/C8SC04228D
COc1ccccc1C(O)CCl
Reaction #197297
DOI: 10.1039/C8SC04228D
Oc1cccc(C=C(Cl)Cl)c1
Reaction #212523
DOI: 10.1039/C8SC04228D
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