Benzenemethanol, 4-(diethylamino)-alpha,alpha-bis[4-(diethylamino)phenyl]-

Base Information

• Chemical Name: Benzenemethanol, 4-(diethylamino)-alpha,alpha-bis[4-(diethylamino)phenyl]-
• CAS No.: 596-49-6
• Molecular Formula: C31H43N3O
• Molecular Weight: 473.702
• European Community (EC) Number: 209-886-5
• DSSTox Substance ID: DTXSID9060495
• Nikkaji Number: J252.483J
• Wikidata: Q81989101
• Mol file: 596-49-6.mol

Synonyms:EINECS 209-886-5;596-49-6;p,p',p''-Tris(diethylamino)trityl alcohol;Benzenemethanol, 4-(diethylamino)-.alpha.,.alpha.-bis[4-(diethylamino)phenyl]-;4-(Diethylamino)-alpha,alpha-bis(4-(diethylamino)phenyl)benzenemethanol;Benzenemethanol, 4-(diethylamino)-alpha,alpha-bis(4-(diethylamino)phenyl)-;tris[4-(diethylamino)phenyl]methanol;DTXSID9060495;SCHEMBL12374438;C31H43N3O

Chemical Property of Benzenemethanol, 4-(diethylamino)-alpha,alpha-bis[4-(diethylamino)phenyl]-

Chemical Property:

• XLogP3: 6.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 12
• Exact Mass: 473.340613004
• Heavy Atom Count: 35
• Complexity: 483

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(CC)C1=CC=C(C=C1)C(C2=CC=C(C=C2)N(CC)CC)(C3=CC=C(C=C3)N(CC)CC)O

Technology Process of Benzenemethanol, 4-(diethylamino)-alpha,alpha-bis[4-(diethylamino)phenyl]-

There total 7 articles about Benzenemethanol, 4-(diethylamino)-alpha,alpha-bis[4-(diethylamino)phenyl]- 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: 68.0%

4-diethylaminophenyllithium + Diethyl carbonate (105-58-8,76619-83-5) → ethyl violet (596-49-6)

Guidance literature:

Reference yield:

leuco ethyl crystal violet (4865-00-3) → ethyl violet (596-49-6)

Guidance literature:

leuco ethyl crystal violet; With chloranil; In ethanol; at 70 ℃; for 2h;

With sodium hydroxide; In ethanol; for 0.0833333h; Heating;

Reference yield:

bis[4-(diethylamino)phenyl][4-(diethylammonio)phenyl]methylium (25275-06-3,47743-68-0) → ethyl violet (596-49-6)

Guidance literature:

With Tris buffer; cetyltrimethylammonim bromide; at 25 ℃; under 750060 Torr; Product distribution; various pressures, and different cationic micelles; kinetic parameters of the alkaline fading reactions, volume changes accompanyning the formation MD complexes, and activation volumes in the process product formation; reaction in nonmicellar systems;

DOI:10.1021/ja00361a002

upstream raw materials:

4,4'-bis(diethylamino)benzophenone

N,N-diethylaniline

bis[4-(diethylamino)phenyl][4-(diethylammonio)phenyl]methylium

Diethyl carbonate

Downstream raw materials:

ethyl violet

C₁₈H₂₉O₃S^(1-)*C₃₁H₄₂N₃⁽¹⁺⁾

Refernces

• 1、 -. "Colorant compounds". Page/Page column 32; 33. . Retrieved 2008/12/07.
• 2、 Gupta, Susanta K. Sen,Arvind, Udai. "Carbenium ion-carbinol equilibration for basic triarylmethane dyes: Relative reactivities of dyes in aq. solutions". . p. 998 - 1000. Retrieved 2007/10/02.