N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate

Base Information

Chemical Name:N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate
CAS No.:145441-33-4
Molecular Formula:C₁₇H₁₈F₁₇NO₂
Molecular Weight:591.308
Hs Code.:
DSSTox Substance ID:DTXSID90163037
Wikidata:Q83031883

Synonyms:N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate;1-Undecanaminium, N-(3-carboxypropyl)-N,N-dimethyl-4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-, hydroxide, inner salt;145441-33-4;DTXSID90163037;C17H18F17NO2;C17-H18-F17-N-O2;LS-158393

Suppliers and Price of N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate

Chemical Property:

XLogP3:7.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:19
Rotatable Bond Count:13
Exact Mass:591.1066076
Heavy Atom Count:37
Complexity:799

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+](C)(CCCC(=O)[O-])CCCC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F

Technology Process of N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate

There total 4 articles about N,N-Dimethyl-N-(3-F-octylpropyl)-4-ammoniobutanoate 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:

: 34598-33-9
4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecanoic acid

: 145441-33-4
N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniobutanoate

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / SOCl₂ / Heating

2: 92 percent / diethyl ether / 2 h / Heating

3: 82 percent / LiAlH₄ / diethyl ether / 48 h / Ambient temperature

4: 2.) Amberlite (OH^- form) / 1.) chloroform, reflux, 8 days, 2.) water, methanol

With lithium aluminium tetrahydride; thionyl chloride; Amberlite (OH^- form); In diethyl ether;
DOI:10.1016/0223-5234(92)90020-2

Reference yield:

: 89373-67-1
4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecanoylchloride

: 145441-33-4
N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniobutanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / diethyl ether / 2 h / Heating

2: 82 percent / LiAlH₄ / diethyl ether / 48 h / Ambient temperature

3: 2.) Amberlite (OH^- form) / 1.) chloroform, reflux, 8 days, 2.) water, methanol

With lithium aluminium tetrahydride; Amberlite (OH^- form); In diethyl ether;
DOI:10.1016/0223-5234(92)90020-2

Reference yield:

: 148171-80-6
N,N-dimethyl 3-(F-octyl)-propanamide

: 145441-33-4
N,N-dimethyl, N-(3-F-octyl propyl)-4-ammoniobutanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / LiAlH₄ / diethyl ether / 48 h / Ambient temperature

2: 2.) Amberlite (OH^- form) / 1.) chloroform, reflux, 8 days, 2.) water, methanol

With lithium aluminium tetrahydride; Amberlite (OH^- form); In diethyl ether;
DOI:10.1016/0223-5234(92)90020-2