Substructure Search

[Na]

Cn1c(=O)n(CP(C)(C)=O)c(=O)c2c1ncn2P(C)(C)=O
Reaction #2140
[1-(7-Dimethylphosphinyl-3-methylxanthin-1-yl)methyl]dimethylphosphine Oxide
DOI: 10.6084/m9.figshare.5104873.v1
CSCc1ccc(C(=O)c2ccc(Cl)cc2)cc1
Reaction #2195
desired product
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2cc(Br)ccc2c(O)c1C(=O)OCC
Reaction #3217
title compound
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2c(Cl)cccc2c(O)c1C(=O)OCC
Reaction #3219
solid
Yield 43.8%DOI: 10.6084/m9.figshare.5104873.v1
[Na].c1ccc2ccccc2c1
Reaction #8649
Sodium naphthalene
DOI: 10.6084/m9.figshare.5104873.v1
[Na].c1ccc2ccccc2c1
Reaction #11286
Sodium naphthalene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCc2cc(C(=O)CBr)ccc2O1
Reaction #42732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[N+]1=C(/C=C/C=C/C=C2/N(CCCS(=O)(=O)O)c3ccc(S(=O)(=O)O)cc3C2(C)CCCC(=O)O)C(C)(CCCS(=O)(=O)O)c2cc(S(=O)(=O)O)ccc21.[Na+].[Na+].[Na+]
Reaction #48896
2-{(1E,3E)-5-[3-(3-carboxy-propyl)-3-methyl-5-sulfo-1-(3-sulfo-propyl)-1,3-dihydro-indole-(2E)-ylidene]-penta-1,3-dienyl}-1-ethyl-3-methyl-5-sulfo-3-(3-sulfo-propyl)-3H-indolium trisodium salt
DOI: 10.6084/m9.figshare.5104873.v1
CC1(CCCS(=O)(=O)O)C(/C=C/C=C/C=C2/N(CCCS(=O)(=O)O)c3ccc(S(=O)(=O)O)cc3C2(C)CCCC(=O)O)=[N+](CCCS(=O)(=O)O)c2ccc(S(=O)(=O)O)cc21.[Na+].[Na+].[Na+].[Na+]
Reaction #48897
2-{(1E,3E)-5-[3-(3-carboxy-propyl)-3-methyl-5-sulfo-1-(3-sulfo-propyl)-1,3-dihydro-indole-(2E)-ylidene]-penta-1,3-dienyl}-3-methyl-5-sulfo-1,3-bis-(3-sulfo-propyl)-3 H-indolium tetrasodium salt
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50383
compound XI
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(-c2ccc(C(F)(F)F)cc2)ccc1C#N
Reaction #53576
2-methylthio-4-(4-trifluoromethylphenyl)benzonitrile
Yield 75.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(=O)oc2cc(O)ccc12
Reaction #54975
4-Carbethoxy-7-hydroxy-coumarin
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55739
3-chloro-benzamido
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(O)NC1(c1ccccc1)c1ccccc1
Reaction #56343
Diphenylhydantoin
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CCCN(C(=O)OC(C)(C)C)C1
Reaction #58684
3-methyl-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester
Yield 95.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59905
title compound
Yield 8.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)OCC(COc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)CO1.[Na]
Reaction #59908
title compound
Yield 9.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCCCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59912
title compound
Yield 8.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OC2COC(C)(C)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59913
title compound
Yield 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OC2CCC3(CC2)OCCO3)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59914
title compound
Yield 7.3%DOI: 10.6084/m9.figshare.5104873.v1
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