butane-1-thiol

CCCCSC(=S)SC(C)C(=O)O
Reaction #48461
title compound
المردود 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #48463
crystals
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(CC)(c1ccc(O)cc1)c1ccc(O)cc1
Reaction #63710
3,3-Bis(p-hydroxyphenyl)pentane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1
Reaction #63711
bisphenol A
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1cc(C2(c3ccc(O)c(C)c3)CCCCC2)ccc1O
Reaction #63712
1,1-Bis(3-methyl-4-hydroxyphenyl)cyclohexane
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCSC1CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74971
6-butylthio-1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCCCSc1c(F)c(F)c(C#N)c(F)c1C#N
Reaction #93737
desired compound
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCCCSc1c(F)c(F)c(C#N)c(F)c1C#N
Reaction #181057
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCSc1cc(-n2cc(C)c3c2CC(C)(C)CC3=O)cc2ncnc(N)c12
Reaction #181753
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCSC1=C(C(=O)O)C(c2ccc3c(c2)OCO3)Oc2ccc(OC(C)C)cc21
Reaction #183907
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCSC=C1CCOC1=O
Reaction #205605
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
—
Reaction #214841
29.5
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCSC1(c2ccc(-c3ccccc3)cc2)CC(C(=O)OC)N(C(=O)OCc2ccccc2)C1
Reaction #230670
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCSC=C1CCCC(CC)C1=O
Reaction #234717
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCSc1cc([N+](=O)[O-])cc(C(O)=NC)c1C(=O)O
Reaction #237217
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCSc1c(-c2ccccc2)nn(C)c1-c1ccccc1
Reaction #238003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Oc1cccc(-n2nc(-c3ccccc3)c3cccnc32)c1
Reaction #241675
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCSc1ccc2nn(-c3cc(C(C)(C)C)cc(C(C)(C)C)c3O)nc2c1
Reaction #247260
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCSc1cc(C(=O)Nc2nc3c(OC)ccc(N4CCOCC4)c3s2)ccn1
Reaction #271993
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCSc1c(C#N)cnc2ccc(I)cc12
Reaction #278644
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي