類似構造検索

NCc1ccc2c(c1)OCO2

NCCCc1ccc2c(c1)OCO2
Reaction #5122
3-(3,4-methylenedioxyphenyl) propylamine
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC=Cc1ccc2c(c1)OCO2
Reaction #9398
isosafrole
収率 98652.6%DOI: 10.6084/m9.figshare.5104873.v1
ClCc1ccc2c(c1)OCO2
Reaction #46157
5-chloromethyl benzo[1,3]dioxol
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccc2c(c1)OCO2)C(=O)c1ccccc1
Reaction #46158
2-benzo[1,3]dioxol-5-ylmethyl-3-oxo-3-phenylpropionate ethyl ester
収率 76.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(c2ccc3c(c2)OCO3)CC1
Reaction #46176
solid
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(O)c(O)c1
Reaction #46204
(3,4-dihydroxy-phenyl)-acetonitrile
収率 54.1%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)C1CCCN(Cc2ccc3c(c2)OCO3)C1
Reaction #49672
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)O)C(=O)OC(C)(C)C.NC(=O)c1ccc2c(c1)OCO2
Reaction #51462
N-Boc sarcosine piperonyl amide
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc2c(c1)OCO2)c1ccc2ccn(-c3ccnc(-n4ccnc4)n3)c2c1
Reaction #51465
N-[(1,3-benzodioxol-5-yl)methyl]-1-[2-(1H-imidazol-1-yl)pyrimidin-4-yl]indole-6-carboxamide
収率 4.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cn(-c2nccc(N3CCCCC3CCOCc3ccc4c(c3)OCO4)n2)cn1
Reaction #51468
4-[2-[[(1,3-benzodioxol-5-yl)methoxy]ethyl]piperidin-1-yl]-2-(1H-imidazol-1-yl)pyrimidine
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)NCCc1ccc2c(c1)OCO2
Reaction #51477
2-chloro-N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide
収率 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CCC#N)CC(=O)NCCc1ccc2c(c1)OCO2
Reaction #51479
2-[(2-cyanoethyl)(dimethylethoxycarbonyl)amino]-N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide
収率 88.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCN)Cc1ccc2c(c1)OCO2
Reaction #51480
N-(1,3-benzodioxol-5-ylmethyl)-N-methyl-1,3-propanediamine
DOI: 10.6084/m9.figshare.5104873.v1
CO.ClCCl.[NH4+].[OH-]
Reaction #51481
CH2Cl2 MeOH ammonium hydroxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1CC(O)CN1CCN(CC(=O)Nc2c(C)cccc2C)CC1
Reaction #51642
compound 10
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C)c1NC(=O)CN1CCN(CC(O)Cc2ccccc2)CC1
Reaction #51643
compound 12
DOI: 10.6084/m9.figshare.5104873.v1
OC(=S)CCc1ccc2c(c1)OCO2
Reaction #55092
said acid
収率 52.8%DOI: 10.6084/m9.figshare.5104873.v1
OC(=S)CCc1ccc2c(c1)OCO2
Reaction #56461
said acid
収率 52.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(c2ccc3c(c2)OCO3)CC1
Reaction #67401
solid
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(c2ccc3c(c2)OCO3)CC1
Reaction #67719
solid
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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