2-methylheptane

COc1ccc2[nH]c(S(=O)Cc3ncc(C)c(OC)c3C)nc2c1
Reaction #233283
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCC=CC=CC=CC=CC=CC(=O)OCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C
Reaction #251745
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCNCC1COc2cccc(F)c2O1
Reaction #255707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(C(=O)Cl)ccc1[N+](=O)[O-]
Reaction #264043
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCC=CC=CC=CC=CC=CC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C
Reaction #283560
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(CNCC(O)c1ccccc1)OCc1ccccc1
Reaction #291765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1ccccc1
Reaction #319111
ethylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCCCCCCCCC=CC=CC=CC=CC=CC(=O)OCC=C(C)CCC=C(C)CCC=C(C)C
Reaction #374458
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
NC(=O)c1ccc(Oc2ccc(CCNCc3ccccc3)cc2)nc1
Reaction #392433
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)OCC1OC(OCCSc2ccc(N)cc2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #398445
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCC(C)C
Reaction #708155
2-methylheptane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
CCCCCCCCCC=CC=CC=CC=CC=CC(=O)OCC=C(C)CCC=C(C)C
Reaction #751046
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(=O)OCC1OC(OCCSc2ccc([N+](=O)[O-])cc2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #780393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCCC(C)C
Reaction #790496
2-methylheptane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_01
CC(C)(N)Cc1ccc(Oc2ccc(C(N)=O)cn2)cc1
Reaction #893922
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCN1CCCC1CNC(=O)c1c(O)c(Cl)cc(Cl)c1OC
Reaction #902625
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(CC(=O)C(F)F)c1ccc(Br)s1
Reaction #922665
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
OCC1OC1c1ccccc1
Reaction #924112
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
N#CC(c1ccccc1)(c1ccccc1)C1CN(C2CCCCC2)C1
Reaction #1215012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC=C(c1ccccc1)c1ccccc1
Reaction #1218567
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
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