13595-56-7

Basic information

• Product Name: Phosphine, phenyl-, dilithium salt
• CAS NO: 13595-56-7
• Molecular Formula: C6H7P.2Li
• Molecular Weight: 121.961
• Mol File: 13595-56-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phosphine, phenyl-, dilithium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphine, phenyl-, dilithium salt(13595-56-7)
• EPA Substance Registry System: Phosphine, phenyl-, dilithium salt(13595-56-7)

Safety Data

• Hazardous Substances Data: 13595-56-7(Hazardous Substances Data)

Upstream product

• 917-54-4 methyllithium 
• 638-21-1 phenylphosphane 
• 644-97-3 Dichlorophenylphosphine 
• 75600-55-4 1,2,3,4,5-pentaphenyl-1,2,3-triphospholene 
• 109-72-8 n-butyllithium 

Downstream Products

• 114130-48-2 dimeric (P-B)⁽²⁾-4,5-diethyl-2,5-dihydro-2,2,3-trimethyl-1-phenyl-1,2,5-phosphasilaborole 
• 114130-49-3 dimeric (P-B)⁽²⁾-4,5-diethyl-2,5-dihydro-3-isopropenyl-2,2-dimethyl-1-phenyl-1,2,5-phosphasilaborole 
• 112795-13-8 1-tert-butyl-4-(di-isopropylamino)-2,2-dimethyl-3-phenyl-1,3,2,4-azaphosphasilaboretidine 
• 112795-11-6 1-tert-butyl-2,4-bis(di-isopropylamino)-3-phenyl-1,3,2,4-azaphosphadiboretidine 
• 96331-42-9 Bis-(bis-dimethylamino-boryl)-phenylphosphin 
• 173066-40-5 [C₆H₅P(BN(CH₃)2)2]2 
• 2468-05-5 di-(3-hydroxypropyl)-phenyl-phosphin 
• 3619-93-0 P,P'-Diphenyl-P,P'-diethyl phosphin 
• 2468-08-8 1,1'-phenylphosphanediyl-bis-propan-2-ol 
• 20342-00-1 1-Phenylphosphole 
• 135366-47-1 C₂₅H₂₄NPSi 
• 143251-86-9 7,16-Diphenyl-1,4,10,13-tetraoxa-7,16-diphospha-cyclooctadecane 
• 115952-07-3 (3R,4R)-3,4-dimethoxy-1-phenylphospholane 
• 22836-26-6 bis(3-carboxyphenyl)phenylphosphine 

Relevant articles and documents

Darstellung und Eigenschaften von Cyclohexasilanylderivaten

New derivatives, containing cyclohexasilanyl groups bonded to a variety of non-metallic elements, are described.Undecamethylcyclohexasilanol and the corresponding Li and Na salts, undecamethylcyclohexasilathiol, bis(undecamethylcyclohexasilanyl)-thiane an

Diastereospecific synthesis of phosphinidene-capped cyclodextrins leading to "introverted" ligands

α-Cyclodextrins (α-CDs) containing "PPh" units which cap the primary face of the CD were obtained in high yield by reaction of Li2PPh with A,B- or A,C-dimesylated and A,B,D,E-tetramesylated precursors; the resulting phosphines are diaster-eomer