1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole

Base Information

Chemical Name:1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole
CAS No.:854036-30-9
Molecular Formula:C₂₇H₃₀NP
Molecular Weight:399.516
Hs Code.:
DSSTox Substance ID:DTXSID301190178
Nikkaji Number:J2.172.685K

Synonyms:DTXSID301190178;854036-30-9;1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole

Suppliers and Price of 1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole

Chemical Property:

XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:9
Exact Mass:399.211586959
Heavy Atom Count:29
Complexity:432

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(CP(CCC1=CC=CC=C1)CCC2=CC=CC=C2)N3C=CC4=CC=CC=C43

Technology Process of 1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole

There total 1 articles about 1-[2-[Bis(2-phenylethyl)phosphino]-1-methylethyl]-1H-indole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 89.0%

: 93017-30-2
bis(2-phenethyl)phosphine

: 405150-33-6
1-(prop-1-en-2-yl)-1H-indole

: 854036-30-9
[2-(1H-indol-1-yl)propyl]bis(2-phenylethyl)phosphine

Guidance literature:: With 2,2'-azobis(isobutyronitrile); at 65 ℃; for 48h;
DOI:10.1055/s-2005-861842

Reference yield: 50.0%

: 854036-30-9
[2-(1H-indol-1-yl)propyl]bis(2-phenylethyl)phosphine

: H₄(ruthenium)4(carbonyl)12

: [H₄Ru₄(CO)11([2-(1-indolyl)propyl]di(2-phenylethyl)phosphine)]

Guidance literature:: With (CH₃)3NO*2H₂O; In chloroform; a soln. of 1 equiv of phosphine was syringed into a Schlenk tube containing a deaerated suspn. of H4Ru4(CO)12 in CHCl3, the mixt. was frozen (N2), a soln. of (CH3)3NO*2H2O in CHCl3 was added under Ar, evacuated, warmed to 20°C with stirring; column chromy. (CH2Cl2-methanol, 10:1 v/v); as oily uncrystallizable sample;
DOI:10.1007/s11172-007-0205-y