Lignans and related compounds
9,10-Di(1-naphthayl)anthracene (purified by sublimation) 99.0+%, TCI America™
CAS: 26979-27-1 Molecular Formula: C34H22 Molecular Weight (g/mol): 430.55 MDL Number: MFCD04222155 InChI Key: GWNJZSGBZMLRBW-UHFFFAOYSA-N PubChem CID: 259845 IUPAC Name: 9,10-dinaphthalen-1-ylanthracene SMILES: C1=CC=C2C(=C1)C=CC=C2C3=C4C=CC=CC4=C(C5=CC=CC=C53)C6=CC=CC7=CC=CC=C76
10-(2-Naphthyl)anthracene-9-boronic Acid (contains varying amounts of Anhydride) 98.0+%, TCI America™
CAS: 597554-03-5 Molecular Formula: C24H17BO2 Molecular Weight (g/mol): 348.208 MDL Number: MFCD11973625 InChI Key: YGVDBZMVEURVOW-UHFFFAOYSA-N Synonym: 10-2-naphthyl anthracene-9-boronic acid,10-naphthalen-2-yl anthracen-9-yl boronic acid,boronic acid, 10-2-naphthalenyl-9-anthracenyl,10-naphthalen-2-yl anthracen-9-ylboronic acid,10-2-naphthyl-9-anthrylboronic acid,10-2-naphthyl-9-anthryl boronic acid,10-naphth-2-ylanthracen-9-ylboronic acid,10-naphthalen-2-yl-anthracene-9-boronic acid,10-naphthalene-2-yl-anthracene-9-boronic acid PubChem CID: 23088556 IUPAC Name: (10-naphthalen-2-ylanthracen-9-yl)boronic acid SMILES: B(C1=C2C=CC=CC2=C(C3=CC=CC=C13)C4=CC5=CC=CC=C5C=C4)(O)O
9-Bromo-10-(1,1':3',1″-terphenyl-5'-yl)anthracene 98.0+%, TCI America™
CAS: 474688-74-9 Molecular Formula: C32H21Br Molecular Weight (g/mol): 485.424 MDL Number: MFCD26406220 InChI Key: BQYDXENQXPPQLP-UHFFFAOYSA-N PubChem CID: 23067325 IUPAC Name: 9-bromo-10-(3,5-diphenylphenyl)anthracene SMILES: C1=CC=C(C=C1)C2=CC(=CC(=C2)C3=C4C=CC=CC4=C(C5=CC=CC=C53)Br)C6=CC=CC=C6
![9-Bromo-10-[4-(1-naphthyl)phenyl]anthracene 98.0+%, TCI America™](https://assets.fishersci.com/TFS-Assets/CCG/Chemical-Structures/chemical-structure-cas-1092390-01-6.jpg-250.jpg)
9-Bromo-10-[4-(1-naphthyl)phenyl]anthracene 98.0+%, TCI America™
CAS: 1092390-01-6 Molecular Formula: C30H19Br Molecular Weight (g/mol): 459.386 MDL Number: MFCD20486477 InChI Key: AEIPFESDNDUXNK-UHFFFAOYSA-N PubChem CID: 59861528 IUPAC Name: 9-bromo-10-(4-naphthalen-1-ylphenyl)anthracene SMILES: C1=CC=C2C(=C1)C=CC=C2C3=CC=C(C=C3)C4=C5C=CC=CC5=C(C6=CC=CC=C64)Br
9,10-Di(1-naphthyl)anthracene 98.0+%, TCI America™
CAS: 26979-27-1 Molecular Formula: C34H22 Molecular Weight (g/mol): 430.55 MDL Number: MFCD04222155 InChI Key: GWNJZSGBZMLRBW-UHFFFAOYSA-N PubChem CID: 259845 IUPAC Name: 9,10-dinaphthalen-1-ylanthracene SMILES: C1=CC=C2C(=C1)C=CC=C2C3=C4C=CC=CC4=C(C5=CC=CC=C53)C6=CC=CC7=CC=CC=C76
Sigma Aldrich Rubrene
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.
Sigma Aldrich Rubrene
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.
Sigma Aldrich 5-Nitro-2-furoic 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.
Sigma Aldrich 9,10-Diphenylanthracene
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.
TARGETMOL CHEMICALS INC Etoposide 500MG
Also available in 1 mL, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Etoposide (VP-16-213) is a topoisomerase II inhibitor that inhibits DNA synthesis by forming a complex with topoisomerase II and DNA (IC50=60.3 uM). Etoposide has antitumor activity and induces apoptosis and autophagy. Purity 99.95%
Selleck Chemical LLC Etoposide S1225-10g
Etoposide is a semisynthetic derivative of podophyllotoxin which inhibits DNA synthesis via topoisomerase II inhibition activity which enhances double-strand and single-strand cleavage of DNA and reversibly inhibits repair by topoisomerase II binding Etoposide induces autophagy mitophagy and apoptosis
Cayman Chemical EtoposIde-d3 1mg
An internal standard for the quantification of etoposide by GC- or LC-MS