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Filtered Search Results
2,3:5,6-Di-O-isopropylidene-D-mannofuranose 98.0+%, TCI America™
CAS: 14131-84-1 Molecular Formula: C12H20O6 Molecular Weight (g/mol): 260.286 MDL Number: MFCD00134206 InChI Key: JWWCLCNPTZHVLF-WVHJSVDISA-N Synonym: 2,3:5,6-bis-o-1-methylethylidene-,a-d-mannofuranose,3ar,4s,6r-6-2,2-dimethyl-1,3-dioxolan-4-yl-2,2-dimethyl-tetrahydrofuro 3,4-d 1,3 dioxol-4-ol PubChem CID: 45039045 IUPAC Name: (3aR,4S,6R)-6-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol SMILES: CC1(OCC(O1)C2C3C(C(O2)O)OC(O3)(C)C)C
| PubChem CID | 45039045 |
|---|---|
| CAS | 14131-84-1 |
| Molecular Weight (g/mol) | 260.286 |
| MDL Number | MFCD00134206 |
| SMILES | CC1(OCC(O1)C2C3C(C(O2)O)OC(O3)(C)C)C |
| Synonym | 2,3:5,6-bis-o-1-methylethylidene-,a-d-mannofuranose,3ar,4s,6r-6-2,2-dimethyl-1,3-dioxolan-4-yl-2,2-dimethyl-tetrahydrofuro 3,4-d 1,3 dioxol-4-ol |
| IUPAC Name | (3aR,4S,6R)-6-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-ol |
| InChI Key | JWWCLCNPTZHVLF-WVHJSVDISA-N |
| Molecular Formula | C12H20O6 |
Span 60 (=Sorbitan Monostearate), TCI America™
CAS: 1338-41-6 Molecular Formula: C24H46O6 Molecular Weight (g/mol): 430.63 MDL Number: MFCD00005366,MFCD00005366 InChI Key: HVUMOYIDDBPOLL-IIZJTUPISA-N Synonym: sorbitan stearate,sorbitan stearate inn,span 60 tn,sorbitan monostearate nf PubChem CID: 23725022 IUPAC Name: 2-[(2R,3S,4R)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl octadecanoate SMILES: CCCCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@@H](O)[C@@H]1O
| PubChem CID | 23725022 |
|---|---|
| CAS | 1338-41-6 |
| Molecular Weight (g/mol) | 430.63 |
| MDL Number | MFCD00005366,MFCD00005366 |
| SMILES | CCCCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@@H](O)[C@@H]1O |
| Synonym | sorbitan stearate,sorbitan stearate inn,span 60 tn,sorbitan monostearate nf |
| IUPAC Name | 2-[(2R,3S,4R)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl octadecanoate |
| InChI Key | HVUMOYIDDBPOLL-IIZJTUPISA-N |
| Molecular Formula | C24H46O6 |
Borane - Tetrahydrofuran Complex (8.5% in Tetrahydrofuran, ca. 0.9mol/L), TCI America™
CAS: 14044-65-6 Molecular Formula: C4H11BO Molecular Weight (g/mol): 85.94 MDL Number: MFCD00012429 InChI Key: RMCYTHFAWCWRFA-UHFFFAOYSA-N Synonym: borane-tetrahydrofuran complex,tetrahydrofuran borane,bh3.thf,borane tetrahydrofuran complex solution,borane-d3-thf complex solution,borane-tetrahydrofuran,unii-5ear4err1l,oxolane borane,boron; oxolane,borane thf PubChem CID: 11062302 IUPAC Name: oxolane borane SMILES: B.C1CCOC1
| PubChem CID | 11062302 |
|---|---|
| CAS | 14044-65-6 |
| Molecular Weight (g/mol) | 85.94 |
| MDL Number | MFCD00012429 |
| SMILES | B.C1CCOC1 |
| Synonym | borane-tetrahydrofuran complex,tetrahydrofuran borane,bh3.thf,borane tetrahydrofuran complex solution,borane-d3-thf complex solution,borane-tetrahydrofuran,unii-5ear4err1l,oxolane borane,boron; oxolane,borane thf |
| IUPAC Name | oxolane borane |
| InChI Key | RMCYTHFAWCWRFA-UHFFFAOYSA-N |
| Molecular Formula | C4H11BO |
Sigma Aldrich 6,7-Dimethylquinoline-3-carboxylic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| CAS | 948294-50-6 |
|---|
Sigma Aldrich Diacetone acrylamide
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| Percent Purity | 99% |
|---|---|
| Linear Formula | CH2=CHCONHC(CH3)2 CH2COCH3 |
| CAS | 2873-97-4 |
| Molecular Weight (g/mol) | 169.22 |
| MDL Number | MFCD00008788 |
| Synonym | N-(1,1-Dimethyl-3-oxobutyl)acrylamide |
| RTECS Number | AS3475000 |
| Recommended Storage | Room Temperature |
| Molecular Formula | C9H15NO2 |
| EINECS Number | 220-713-2 |
| Melting Point | 54°C to 56°C |
Sigma Aldrich Borane-ammonia complex
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| Percent Purity | 97% |
|---|---|
| Linear Formula | H3N -+ BH3 |
| CAS | 13774-81-7 |
| Molecular Weight (g/mol) | 30.87 |
| MDL Number | MFCD00075639 |
| Synonym | Amminetrihydroboron; Borazane |
| Recommended Storage | Room Temperature |
| Molecular Formula | H6BN |
SMOLECULE INC
NC3919536 EE-35-OCTADIEN-2-ONE 95
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eMolecules BORANE AMMONIA COMPLEX 100G
5000224481 BORANE AMMONIA COMPLEX 100G
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Medchemexpress LLC Complex III Subunit | 50UL
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Complex III Subunit | 50UL
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Sigma Aldrich Fine Chemicals Biosciences Sorbitan monostearate meets FCC analytical specifications | 1338-41-6 | 10KG
Sorbitan monostearate meets FCC analytical specifications | Mol Wt: 430.62 | 1338-41-6 | 10KG
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eMolecules R-3-AMINOTETRAHYDROFURAN 5G
5000170369 R-3-AMINOTETRAHYDROFURAN 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000733290 TETRAHYDROFURAN-2 5- 500MG
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Sigma Aldrich Fine Chemicals Biosciences Thymidine 5'-monophosphate disodium salt hydrate >=99% | 33430-62-5 | MFCD09039259 | 1G
Thymidine 5'-monophosphate disodium salt hydrate >=99% | Purity: >=99% | 33430-62-5 | MFCD09039259 | 1G
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Medchemexpress LLC HLA-G COMPLEX TETRAM 20UG
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5000187356 HLA-G COMPLEX TETRAM 20UG
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Apexbio Technology LLC Oligomycin Complex 1404-19-9 10mg
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Oligomycin Complex is a mixture composed primarily of Oligomycin A B and C It functions as a mitochondrial ATP synthase inhibitor targeting specifically the F0 subunit to disrupt oxidative phosphorylation via inhibition of ATP generation Oligomycin A exhibits selective inhibition of ATP synthase with reported GI50 at approximately 270 nM By blocking mitochondrial ATP synthesis oligomycin promotes cellular metabolic shift from oxidative phosphorylation to glycolysis In cell culture studies using various cancer cell lines oligomycin treatment has been demonstrated to suppress mitochondrial respiration and can induce apoptosis Additionally oligomycin has been employed in research to examine cellular bioenergetics adaptations mitochondrial-related apoptosis pathways and synergy of chemotherapeutic combinations in vitro
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