類似構造検索

CCCCCCCCS

CCCCCCCCCCCC
Reaction #863
dodecane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2635
title compound
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cccc(N(c2cccc(CCC(=O)OCC)c2)c2ccc(C)c(C)c2)c1
Reaction #3119
N, N-bis[3-(2-ethoxycarbonylethyl)phenyl]-3,4-xylidine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cccc(N(c2ccccc2)c2ccc(-c3ccc(N(c4ccccc4)c4cccc(CCC(=O)OCC)c4)cc3)cc2)c1
Reaction #3120
N,N'-diphenyl-N,N'-bis[3-(2-ethoxycarbonylethyl)phenyl]-[1,1'-biphenyl]-4,4'-diamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(C)=CC(=O)CC1(C)C
Reaction #4075
ester
収率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccccc1.C=Cc1ccccc1C=C
Reaction #5396
Styrene-divinylbenzene
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(P2CCCCCCCC2C2CCCCCCCC2)cc1
Reaction #5736
9-Phenyl-9-Phosphabicyclononane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #5780
4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])[O-].[Al+3].[Mg+2]
Reaction #5859
aluminum-magnesium phosphate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCSC(N)=O
Reaction #6506
S-octadecyl thiocarbamate
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCSCc1ccc(CCl)cc1
Reaction #8518
p-(Octylthiomethyl)benzyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCSCc1ccc(CCl)cc1
Reaction #8519
p-(Octylthiomethyl)benzyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
[Li][c]1cccc2c1ccc1ccccc12
Reaction #8609
1-lithiophenanthrene
DOI: 10.6084/m9.figshare.5104873.v1
[Li][c]1cccc2c1ccc1ccccc12
Reaction #8610
1-lithiophenanthrene
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2cccc(F)c2)C(=O)O1
Reaction #8619
title compound
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc2nc(NC(=O)NCC)sc12
Reaction #9217
desired compound
収率 15.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10717
4-[3-(5-benzo[b]thiophen-2-yl-2,4-dimethoxy-phenyl)-E-acryloyl]-benzoic acid
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC1(CCCCCCCC)c2ccccc2-c2ccc(C(=O)NNC(=O)c3cc(Cl)ccc3Cl)cc21
Reaction #11280
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc(N3CCCCC3)cc2c(-c2ccccc2)c1S(C)(=O)=O
Reaction #41934
solid
収率 398.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc(N3CCOCC3)cc2c(-c2ccccc2)c1S(C)(=O)=O
Reaction #41935
solid
収率 78.6%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ