Substructure Search

CCCCCCCCCCCC

NCC(O)CNC(=O)CCCCCCCCCCCO
Reaction #1220
title compound
Yield 75.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC.C=CN1CCCC1=O
Reaction #1498
lauryl methacrylate N-vinyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCC(=O)OC(C)C
Reaction #1500
isopropyl myristate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCCCCCCCCCCC
Reaction #4991
Dodecyl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCCNC(=O)C(F)(F)F
Reaction #11999
amide
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCS(=O)(=O)Nc1cc(-c2cc3cc(F)c(F)cc3[nH]2)ccc1OC
Reaction #53786
product
Yield 44.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOc1nc(OCCCCCCCCCCCC)nc(Oc2cc(-c3ccccc3)c(O)c(-c3ccccc3)c2)n1
Reaction #54159
6-(4-hydroxy-3,5-diphenylphenoxy)-2,4-dilauroxys-triazine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOc1nc(OCCCCCCCCCCCCCCCCCC)nc(Oc2cc(-c3ccccc3)c(O)c(-c3ccccc3)c2)n1
Reaction #54160
6-(4-hydroxy-3,5-diphenyphenoxy)-2,4-distearoxy-s-triazine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(O)C1
Reaction #62539
menthol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOP(=O)(O)O[C@H](CC(=O)O)C[N+](C)(C)C.[OH-]
Reaction #64412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64421
salt
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC
Reaction #71258
Cetyl Stearate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)O.OCCN(CCO)CCO
Reaction #71259
Triethanolamine Stearate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1ccc(C(C)(CCCCC(=O)CCCCC(C)(C(=O)O)c2ccc(CC(C)C)cc2)C(=O)O)cc1
Reaction #76265
2,12-bis-(4-isobutyl-phenyl)-2,12-dimethyl-7-oxo-tridecanedioic acid
Yield 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(O)CC(=O)OC
Reaction #84018
β-hydroxydodecanoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCCCCCCNC(=O)C(F)(F)F
Reaction #88689
amide
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OCCN(C)C
Reaction #93843
2-dimethylaminoethyl laurate
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCCCCCCCCCCCCO
Reaction #162013
12-Azido-1-dodecanol
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCCCCCCO
Reaction #173302
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOc1cc(OCCCCc2ccc3cc(OCc4ccccc4)c(OCc4ccccc4)cc3c2)cc(N(CC(=O)OC)CC(=O)OC)c1
Reaction #173808
DOI: 10.1039/C8SC04228D
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