部分構造検索

OCCCCCCCCCCBr

CCCCCCCCCCCCc1ccc(N=Nc2ccc(OCCCCCCCCCCBr)cc2)cc1
Reaction #5849
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCc1ccc(N=Nc2ccc(OCCCCCCCCCCBr)cc2)cc1
Reaction #5850
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCc1ccc(N=Nc2ccc(OCCCCCCCCCC[N+](C)(C)CCO)cc2)cc1.[Br-]
Reaction #5851
10-[4-[[4-(dodecyl)phenyl]azo]phenoxy]-N-(2-hvdroxyethyl)-N,N-dimethyl-1-decanaminium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCCC2(C)C(C(C)CC(Cl)CBr)=CCC12
Reaction #6379
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](Br)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40600
36
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N=[N+]=[N-])C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40601
38
収率 87.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(=O)CC[C@@H]12
Reaction #50340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C(Br)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
Reaction #78037
4-Bromo-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(Br)CCCCCCCCCO
Reaction #81777
10-bromo-undecan-1-ol
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCCCCC(C)Oc1cccc(I)c1
Reaction #81778
ethyl 10-(3-iodophenoxy)-undecanoate
収率 33.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(Br)C(=O)C2C1(C)CCC1C(=O)OC(c3ccoc3)CC12C
Reaction #180528
DOI: 10.1039/C8SC04228D
CC(CCCC(C)(O)CO)C1CCC2C3C(Br)C=C4CC(O)CC(O)C4(C)C3CCC12C
Reaction #186987
DOI: 10.1039/C8SC04228D
CC(=O)OCCCCCCCCC(=O)CBr
Reaction #189031
DOI: 10.1039/C8SC04228D
CC(=O)Cc1ccc(OCCCCCCCCCCN2CCC(=O)N2)cc1
Reaction #191568
DOI: 10.1039/C8SC04228D
CC12CCC(O)C=C1CCC1C2C(=O)CC2(C)C(C(=O)CBr)CCC12
Reaction #192455
DOI: 10.1039/C8SC04228D
CC1CCC2(OC1)OC1CC3C4CCC5CC(=O)C=CC5(C)C4CCC3(C)C1C2C
Reaction #200852
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)CBr)C4(C)CCC3C2(C)C(OC(C)=O)C1
Reaction #234477
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(OCCCCCCCCCCCCBr)cc1
Reaction #235025
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2CCC3C(CCC4(C)C(C(C)=O)CCC34)C2(C)CC1Br
Reaction #236903
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2C3CCC4=CC(=O)CCC4(C)C3(Br)C(F)CC12C
Reaction #240015
DOI: 10.1039/C8SC04228D
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