Teilstruktursuche

CCCCCCC(C)O

CCCCC[C@H]1[C@@H](CC(=O)[O-])CC[C@H]1O
Reaction #2467
(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H](O)CC(=O)O
Reaction #5718
(R)-3-hydroxytetradecanoic acid
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C1CCCC2OC2CC1
Reaction #42012
9-oxabicyclo[6.1.0] nonane
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCC(O)CCC1
Reaction #44492
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)NC(C)c3ccc(F)cc3)c2)C1
Reaction #49248
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)NC(C)c3ccc(F)cc3)c2)C1
Reaction #49249
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O
Reaction #52122
(R)-3-hydroxyoctanoyl-CoA
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(O)CC(=O)OCc1ccccc1
Reaction #53260
benzyl 3-hydroxymyristate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(C)(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54875
4-(4-Acetyl-8-hydroxy-8-methyltridecyl)benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54877
final product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(CCCc1ccc(C(=O)O)cc1)CCCC(O)CCCC(C)C
Reaction #54878
final product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(CCCc1ccc(C(=O)O)cc1)CCCC(O)CCCC(C)(C)C
Reaction #54879
4-(4-acetyl-8-hydroxy-12,12-dimethyltridecyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54880
4-(4-acetyl-8-hydroxytridec-12-en-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCOCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54888
4-(4-Acetyl-8-hydroxy-9-propoxynonyl)benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CCCc1ccc(C(=O)OC)cc1)C(C)=O
Reaction #54889
methyl 4-(4-acetyl-8-hydroxytridecyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #54890
ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O)OC(C)=O
Reaction #54891
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CCCc1cccc(C(=O)O)c1)C(C)=O
Reaction #54893
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C)c2c(c(C)c1O)CC[C@@](C)(CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O2
Reaction #55674
α-tocopherol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(N)C(C)O
Reaction #55868
3-amino-2-nonanol
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter