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Research Organics




Product Image Model- Price Item Name
(+)-5-Fluoro-2'-deoxyuridine: Floxuridine ST056942 ST056942 $61.00

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(+)-5-Fluoro-2'-deoxyuridine: Floxuridine ST056942

50919

MFCD00435692

C9H11FN2O5

246.2

(+)-5-Fluoro-2'-deoxyuridine: Floxuridine ST056942Formula: C9H11FN2O5MW: 246.2
SALT: LogP: -1.89LogS: -2.15
Lipinsky: 4Acceptors: 5Donors: 3
Rotation Bonds: 1N+O: 7Chiral Centers: 3
CAS: 50919MDL Number: MFCD00435692
IUPACNAME: 1-[(4S,2R,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-fluoro-1,3-dihydropyri midine-2,4-dione
Smiles: C1[C@@H]([C@@H](CO)O[C@H]1n1c([nH]c(c(c1)F)=O)=O)O

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(+)-5-Iodo-2'-deoxyuridine; Idoxuridine ST041015 ST041015 $61.00

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(+)-5-Iodo-2'-deoxyuridine; Idoxuridine ST041015

54422

MFCD06661895

C9H11IN2O5

354.1

(+)-5-Iodo-2'-deoxyuridine; Idoxuridine ST041015Formula: C9H11IN2O5MW: 354.1
SALT: LogP: -0.26LogS: -2.86
Lipinsky: 4Acceptors: 5Donors: 3
Rotation Bonds: 1N+O: 7Chiral Centers: 3
CAS: 54422MDL Number: MFCD06661895
IUPACNAME: 1-[(4S,2R,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,3-dihydropyrimi dine-2,4-dione
Smiles: C([C@H]1OC([n@]2c([nH]c(c(c2)I)=O)=O)C[C@@H]1O)O

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(+)-6-Aminopenicillanic acid ST055519 ST055519 $61.00

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(+)-6-Aminopenicillanic acid ST055519

551-16-6

MFCD03225429

C8H12N2O3S

216.26


IDENTIFIER
IDNUMBERNAMECASMDL
ST055519(+)-6-Aminopenicillanic acid551-16-6MFCD03225429
IUPACNAME
(2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carb oxylic acid
Smiles
N12C(SC([C@@H]2C(=O)O)(C)C)C(C1=O)N
Chem-Physical
FormulaMolecular WeightSALT
C8H12N2O3S216.26
LogPLogSLipinskyAcceptors
-0.89-2.3443
DonorsRotation BondsChiral CentersN+O
3135
SOURCE
Obtained from cultures of Penicillium chrysogenum
REFERENCE
Merck 13, 457

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(+)-alpha-Tocopherol acid succinate ST075423 ST075423 $61.00

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(+)-alpha-Tocopherol acid succinate ST075423

MFCD00198020

C33H54O5

530.79


IDENTIFIER
IDNUMBERNAMECASMDL
ST075423(+)-alpha-Tocopherol acid succinate893081MFCD00198020
IUPACNAME
3-{[(2R)-2-((4R,8R)-4,8,12-trimethyltridecyl)-2,5,7,8-tetramethylchroman-6-yl] oxycarbonyl}propanoic acid
Smiles
Cc1c2c(c(c(c1C)OC(CCC(=O)O)=O)C)CC[C](O2)(CCC[C@@H](CCC[C@@H](CCCC(C)C)C)C)C
Chem-Physical
FormulaMolecular WeightSALT
C33H54O5530.79
LogPLogSLipinskyAcceptors
12.27-8.2325
DonorsRotation BondsChiral CentersN+O
11835
SOURCE
Naturally occurring form of vitamin E; Richest sources are green vegetables, grains, and oils, particularly palm, safflower and sunflower oils. Isoln from wheat germ
REFERENCE
Merck 13, 9571

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(+)-Bicuculline ST057559 ST057559 $61.00

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(+)-Bicuculline ST057559

485494

MFCD00067279

C20H17NO6

367.36


IDENTIFIER
IDNUMBERNAMECASMDL
ST057559(+)-Bicuculline485-49-4MFCD00067279
IUPACNAME
(6R)-6-((5S)-6-methyl(5,6,7,8-tetrahydro-2H-1,3-dioxolano[4,5-g]isoquinolin-5- yl))-6-hydro-2H-1,3-dioxoleno[4,5-e]isobenzofuran-8-one
Smiles
c12c(c3C(O[C@H](c3cc2)([C@@H]2(c3cc4OCOc4cc3CCN2C)))=O)OCO1
Chem-Physical
FormulaMolecular WeightSALT
C20H17NO6367.36
LogPLogSLipinskyAcceptors
2.62-4.3446
DonorsRotation BondsChiral CentersN+O
0127
SOURCE
found in Dicentra cucullaria (L.) Bernh., Adlumia fungosa (Ait.) Greene, Fumariaceae, and several Corydalis species
REFERENCE
Merck 13, 1207

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(+)-Cinchonine ST056305 ST056305 $61.00

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(+)-Cinchonine ST056305

118-10-5

MFCD00180253

C19H22N2O

294.4


IDENTIFIER
IDNUMBERNAMECASMDL
ST056305(+)-Cinchonine118-10-5MFCD00180253
IUPACNAME
((5R)-5-vinylquinuclidin-2-yl)(1S)-4-quinolylmethan-1-ol
Smiles
c1(ccnc2c1cccc2)[C@@H]([C@H]1(CC2CC[N@@]1C[C@@H]2(C=C)))O
Chem-Physical
FormulaMolecular WeightSALT
C19H22N2O294.4HCl, H2O
LogPLogSLipinskyAcceptors
3.56-4.5341
DonorsRotation BondsChiral CentersN+O
1343
SOURCE
Occurs in most varieties of cinchona bark, especially in bark of Cinchona micrantha, Rubiaceae
REFERENCE
Merck 13, 2308

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(+)-Dehydroabietylamine ; Leelamine ST056281 ST056281 $61.00

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(+)-Dehydroabietylamine ; Leelamine ST056281

1446-61-3

MFCD05618226

C20H31N

285.47


IDENTIFIER
IDNUMBERNAMECASMDL
ST056281(+)-Dehydroabietylamine ; Leelamine1446-61-3MFCD05618226
IUPACNAME
[(4aS,1R,10aR)-1,4a-dimethyl-7-(methylethyl)-1,2,3,4,9,10,10a,4a-octahydrophen anthryl]methylamine
Smiles
c12[C]3(C(C(CN)(C)CCC3)CCc1cc(cc2)C(C)C)C
Chem-Physical
FormulaMolecular WeightSALT
C20H31N285.47
LogPLogSLipinskyAcceptors
7.19-5.5530
DonorsRotation BondsChiral CentersN+O
2131
SOURCE
a main ingredient of rosin amine, isolated from Rosin Gum
REFERENCE

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(+)-Dibenzoyl-D-tartaric acid ST080688 ST080688 $36.00

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(+)-Dibenzoyl-D-tartaric acid ST080688

17026-42-4

MFCD06670634

C18H14O8

358.3

(+)-Dibenzoyl-D-tartaric acid ST080688Formula: C18H14O8MW: 358.3
SALT: LogP: 2.36LogS: -3.93
Lipinsky: 4Acceptors: 8Donors: 2
Rotation Bonds: 9N+O: 8Chiral Centers: 2
CAS: 17026-42-4MDL Number: MFCD06670634
IUPACNAME: 2,3-bis(phenoxycarbonyl)butanedioic acid
Smiles: c1(ccccc1)OC(C(C(C(O)=O)C(=O)Oc1ccccc1)C(O)=O)=O

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(+)-Emetine dihydrochloride hydrate ST056340 ST056340 $61.00

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(+)-Emetine dihydrochloride hydrate ST056340

316-42-7

MFCD04220906

C29H40N2O4

480.65


IDENTIFIER
IDNUMBERNAMECASMDL
ST056340(+)-Emetine dihydrochloride hydrate313222-95-6
IUPACNAME
(1R)-1-[((10S,11aS,9R)-9-ethyl-2,3-dimethoxy(5,6,7,11a-tetrahydropiperidino[2, 1-a]isoquinolin-10-yl))methyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline, c hloride, hydrate
Smiles
c12[C@H]3(N(CC([C@H](C[C@@H]4(c5cc(c(OC)cc5CCN4)OC))C3)CC)CCc2cc(OC)c(c1)OC).Cl.O
Chem-Physical
FormulaMolecular WeightSALT
C29H43ClN2O5535.12
LogPLogSLipinskyAcceptors
5.49-5.9535
DonorsRotation BondsChiral CentersN+O
3647
SOURCE
Derivative of Emetine, which is principal alkaloid of ipecac, the ground roots of Uragoga ipecacuanha
REFERENCE
Merk 13, 3591

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(+)-Isocorydine; artabotrine; luteanine ST057169 ST057169 $61.00

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(+)-Isocorydine; artabotrine; luteanine ST057169

475-67-2

MFCD01844805

C20H23NO4

341.41


IDENTIFIER
IDNUMBERNAMECASMDL
ST057169(+)-Isocorydine; artabotrine; luteanine475-67-2MFCD01844805
IUPACNAME
Smiles
c12c(C[C@H]3(c4c1c(c(cc4CCN3C)OC)OC))ccc(c2O)OC
Chem-Physical
FormulaMolecular WeightSALT
C20H23NO4341.41
LogPLogSLipinskyAcceptors
4.13-4.6544
DonorsRotation BondsChiral CentersN+O
1415
SOURCE
From tubers of Corydalis cava (L.) Schweigg. & Korte (C. tuberosa DC., Fumariaceae); Artabotrys suaveolens Blume, Anonaceae; Papaver oreophilum Rupr.; Phoebe clemensii Allen (Lauraceae) and others
REFERENCE
Merck 13, 5180

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