29680-76-0

Basic information

• Product Name: Phosphonium, [[3,5-bis(acetyloxy)phenyl]methyl]triphenyl-, bromide
• CAS NO: 29680-76-0
• Molecular Formula: C29H26O4P.Br
• Molecular Weight: 549.401
• Mol File: 29680-76-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phosphonium, [[3,5-bis(acetyloxy)phenyl]methyl]triphenyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium, [[3,5-bis(acetyloxy)phenyl]methyl]triphenyl-, bromide(29680-76-0)
• EPA Substance Registry System: Phosphonium, [[3,5-bis(acetyloxy)phenyl]methyl]triphenyl-, bromide(29680-76-0)

Safety Data

• Hazardous Substances Data: 29680-76-0(Hazardous Substances Data)

Upstream product

• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 20982-28-9 5-methylbenzene-1,3-diyl diacetate 
• 504-15-4 orcinol 
• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 108-24-7 acetic anhydride 
• 603-35-0 triphenylphosphine 
• 104311-39-9 5-(bromomethyl)-1,3-phenylene diacetate 
• 33617-40-2 5-(bromomethyl)benzene-1,3-diol 

Downstream Products

• 10083-24-6 trans-piceatannol 
• 500-65-2 rhapontigenin 
• 33626-09-4 (E)-3,3',5,5'-tetrahydroxystilbene 
• 4721-07-7 oxyresveratrol 
• 32507-66-7 isorhapontigenin 
• 113681-38-2 2',4'-dibromo-3,3',4,5'-tetramethoxystilbene 
• 113681-39-3 (E)-2'-bromo-3,3'4,5'-tetramethoxystilbene 
• 110993-17-4 dimethoxycarbonyloxy-3',5' methoxy-4'' diphenyl-1,2 ethane 
• 110993-16-3 Acetic acid 3-acetoxy-5-[2-(4-methoxy-phenyl)-ethyl]-phenyl ester 
• 90332-29-9 α,β-dihydro-3,5-dihydroxy-4'-methoxystilbene 
• 1018449-53-0 3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene 
• 29680-77-1 (3,5-dihydroxybenzyl)triphenylphosphonium bromide 
• 33620-66-5 Acetic acid 3-acetoxy-5-[(E)-2-(4-methoxy-phenyl)-vinyl]-phenyl ester 

Relevant articles and documents

Biomimetic preparation of the racemic modifications of the stilbenolignan aiphanol and three congeners

A chromatographically separable mixture of the racemic modification, (±)-1, of the stilbenolignan (-)-aiphanol and congeners (±)-2-4 has been generated by a silver(I)-mediated and potentially biomimetic oxidative coupling of piceatannol (5) with sinapic a

SYNTHESIS OF CONDENSED TANNINS. PART 18. STILBENES AS POTENT NUCLEOPHILES IN REGIO- AND STEREO-SPECIFIC CONDENSATIONS: NOVEL GUIBOURTINIDOL-STILBENES FROM GUIBOURTIA COLEOSPERMA

(E)-3,3',4,5'-Tetrahydroxy- and 3',4,5'-trihydroxy-stilbenes function as strong nucleophiles in regio- and stereo-specific condensations with carbenium ions generated from 2,3-trans- and 2,3-cis-flavan-3,4,4',7-tetraols (leucoguibourtinidins) to generate