boric acid

CC(C)CC(C)OB(OC(C)CC(C)C)OC(C)CC(C)C
Reaction #4966
Tri(4-methyl-2-pentyl) Borate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1c[nH]c(-c2nc3ccccc3o2)c1
Reaction #6525
2-(pyrrol-2-yl)benzoxazole
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1c[nH]c(-c2nc3ccccc3s2)c1
Reaction #6526
2-(pyrrol-2-yl)benzothiazole
Ausbeute 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCNC(=O)Nc1nc2ccc(-c3cccc(N)c3)cc2s1
Reaction #9241
desired compound
Ausbeute 23.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #54828
diazonium salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
COCCCNc1cc(O)c2c(c1O)C(=O)c1ccccc1C2=O
Reaction #63176
2-(methoxypropylamino)-1,4-dihydroxyanthraquinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(=O)N(CC(O)CCCCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I
Reaction #70106
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N(CC(O)COCCOCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I
Reaction #70107
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N(CC(O)CC1(O)CC(CO)OC(CN(C(C)=O)c2c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c2I)C1)c1c(I)c(C(=O)N(CCO)CCO)c(I)c(C(=O)N(CCO)CCO)c1I
Reaction #70108
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N(CC(O)CCCCC(O)CN(C(C)=O)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I
Reaction #70109
5,5′-(2,7-dihydroxyoctane-1,8-diyl)bis(acetylazanediyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N(CC(O)CCCCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(C)CC(O)CO)c(I)c(C(=O)N(C)CC(O)CO)c1I)c1c(I)c(C(=O)N(C)CC(O)CO)c(I)c(C(=O)N(C)CC(O)CO)c1I
Reaction #70110
5,5′-(2,7-dihydroxyoctane-1,8-diyl)bis(acetylazanediyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-N1,N3-dimethylisophthalamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N(CC(O)COCCOCC(O)CN(C(C)=O)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I
Reaction #70111
5,5′-(5,12-dihydroxy-2,15-dioxo-7,10-dioxa-3,14-diazahexadecane-3,14-diyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide)
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N(CC(O)COCCOCC(O)CN(C(C)=O)c1c(I)c(C(=O)N(C)CC(O)CO)c(I)c(C(=O)N(C)CC(O)CO)c1I)c1c(I)c(C(=O)N(C)CC(O)CO)c(I)c(C(=O)N(C)CC(O)CO)c1I
Reaction #70112
5,5′-(5,12-dihydroxy-2,15-dioxo-7,10-dioxa-3,14-diazahexadecane-3,14-diyl)bis(N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-N1,N3-dimethylisophthalamide)
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCCCCCCCCCCCCNc1ccc(O)c2c1C(=O)c1c(N)ccc(N)c1C2=O
Reaction #93823
1,4-diamino-5-hydroxy-8-palmitylaminoanthraquinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCC(C)(C)c1ccc2oc(-c3ccc(O)cc3)nc2c1
Reaction #159254
product
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1ccc(CC(=O)NC(CC(C)C)c2ccccc2N2CCCCC2)cc1OCC
Reaction #187918
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)Cc1ccc(OC(=O)c2ccc(O)cc2Cl)cc1
Reaction #189655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc2c(c(O)c1C=O)CCCC2
Reaction #190795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)CNC(=O)Cc1ccc(Cl)cc1
Reaction #206740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1[nH]c(=O)c2nc3cc(Cl)c(Cl)cc3nc2[nH]1
Reaction #213950
7,8-dichloro-alloxazine
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
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