Lithium, (2,2-diphenylethenyl)-

Base Information

Chemical Name:Lithium, (2,2-diphenylethenyl)-
CAS No.:29619-50-9
Molecular Formula:C14H11Li
Molecular Weight:186.182
Hs Code.:
DSSTox Substance ID:DTXSID70452537
Mol file:29619-50-9.mol

Synonyms:Lithium, (2,2-diphenylethenyl)-;29619-50-9;DTXSID70452537

Suppliers and Price of Lithium, (2,2-diphenylethenyl)-

Supply Marketing:

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

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Chemical Property of Lithium, (2,2-diphenylethenyl)-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:186.10207879
Heavy Atom Count:15
Complexity:166

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:[Li+].[CH-]=C(C1=CC=CC=C1)C2=CC=CC=C2

Technology Process of Lithium, (2,2-diphenylethenyl)-

There total 1 articles about Lithium, (2,2-diphenylethenyl)- 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: 90.0%

: 76557-96-5
trimethyl-β-(phenylstyryl)stannane

: 29619-50-9
1-lithio-2,2-diphenylethylene

Guidance literature:: With methyllithium; In tetrahydrofuran; for 2h;
DOI:10.1021/jo00303a022

Reference yield:

: 29619-50-9
1-lithio-2,2-diphenylethylene

: 74-88-4
methyl iodide

: 778-66-5
1,1-diphenyl-1-propene

: 1450-63-1
1,1,4,4-tetraphenyl-1,3-butadiene

Guidance literature:: Multistep reaction; 1) 125 deg C, 24 h;
DOI:10.1021/jo00303a022

Reference yield:

: 29619-50-9
1-lithio-2,2-diphenylethylene

: 1027386-09-9
2-(2,2-diphenyl-vinyl)-4,4-dimethoxy-3-(2-vinyl-cyclohex-1-enyl)-cyclobut-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) TFAA

2: tetrahydrofuran / -78 °C

With trifluoroacetic anhydride; In tetrahydrofuran;
DOI:10.1021/jo982422l