Substructure Search

2838

CCOC(=O)C(=O)CC(=O)c1c(C)cc(C)cc1C
Reaction #1248
red oil
Yield 66.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)[O-].[K+]
Reaction #4059
Potassium ethyl oxalate
Yield 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(Cc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5440
desired product
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CCc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5449
desired product
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6499
2-ethoxalyloxyethyl methacrylate
Yield 76.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6500
2-ethoxalyloxyethyl methacrylate
Yield 76.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6501
2-ethoxalyloxyethyl methacrylate
Yield 56.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCOC(=O)C(=O)OCC
Reaction #6502
2-ethoxalyloxyethyl methacrylate
Yield 73.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(CCOC(=O)C(=O)OCC)cc1
Reaction #6503
aimed compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc2ccccc21
Reaction #6798
N-ethyl-indole
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)CNC(=O)C(=O)OCC
Reaction #46264
title material
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Cc1cc(OC2CCN(C(=O)OC(C)(C)C)CC2)ccc1[N+](=O)[O-]
Reaction #48169
4-[3-(2-Ethoxycarbonyl-2-oxo-ethyl)-4-nitro-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(-c2ccccc2)c2c1Cc1ccc(NS(=O)(=O)c3ccc(C)cc3)cc1-2
Reaction #49827
1,4-dihydro-1-phenyl-7-tosylamino -indeno[1,2-c]pyrazole-3-carboxylic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2ccccc2s1
Reaction #50939
ethyl 2-benzothiazolecarboxylate
Yield 36.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCc2ccccc2)ccc2c(=O)cc(C(=O)O)oc12
Reaction #51609
8-methyl-4-oxo-7-(phenylmethoxy)-4H-1-benzopyran-2-carboxylic acid
Yield 95.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Cc1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #51772
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+](=O)[O-])c1CC(=O)O
Reaction #52584
2-methyl-6-nitrophenylacetic acid
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CC(=O)O)CC=CC=C1[N+](=O)[O-]
Reaction #52781
1-methyl-6-nitrophenylacetic acid
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1nc2ccccc2s1
Reaction #54746
desired product
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc2ccccc21
Reaction #56694
N-ethyl-indole
DOI: 10.6084/m9.figshare.5104873.v1
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