2-chloroethyl methyl ether

COCCOC(=O)c1cncn1C1CCCc2ccccc21
Reaction #5879
(2-methoxyethyl) 1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole-5-carboxylate
Rendimiento 46.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COCCN(C)CCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11574
titled compound
Rendimiento 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCCN(C)CCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #46686
compound
Rendimiento 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCOc1ccc2c(c1)CN(C(=O)c1cc(C(C)C)c(OCc3ccccc3)cc1OCc1ccccc1)C2
Reaction #69698
title compound
Rendimiento 104.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCCOc1cccc2ccccc12
Reaction #70121
1-(2-methoxyethoxy)naphthalene
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCCS(=O)(=O)[O-]
Reaction #187472
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCOc1cccc(Br)c1
Reaction #188811
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCN1CCC(Oc2ccc(CN3CCN(C(=O)c4ccccc4)CC3)cc2)CC1
Reaction #188847
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCOc1cccc(Br)c1
Reaction #195548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCOc1c([N+](=O)[O-])ccc(C(=O)OC)c1C
Reaction #199934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCOc1ccc(C=O)cc1
Reaction #200270
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCN1CCC(=Cc2ccccc2OC)C1=O
Reaction #200493
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCn1c(N2CCCN(C(=O)OC(C)(C)C)CC2)nc2ccccc21
Reaction #207124
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cccc(C)c1N(C(=O)CCl)C(C)OC
Reaction #215243
N-(1-methoxy-1-ethyl)-2'-methyl-6'-ethyl-2-chloroacetanilide
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COCCOc1ccc(Br)cc1
Reaction #233502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCn1c(C)cc2c(C(F)(F)F)c(C#N)ccc21
Reaction #234557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN(CC)CCOC
Reaction #243452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCN(C)S(=O)(=O)c1ccc(-c2ncnc3ccc(-c4cn(C(c5ccccc5)(c5ccccc5)c5ccccc5)nc4-c4ccc(F)cc4)cc23)s1
Reaction #251355
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCn1cnc2ccccc21
Reaction #253101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCCOc1ccc([N+](=O)[O-])cc1I
Reaction #253853
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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