4-[2-(4-Chlorophenyl)ethenyl]-1-ethylpyridin-1-ium

Base Information

Chemical Name:4-[2-(4-Chlorophenyl)ethenyl]-1-ethylpyridin-1-ium
CAS No.:6662-59-5
Molecular Formula:C₂₅H₄₀ClNO₂
Molecular Weight:422.051
Hs Code.:
DSSTox Substance ID:DTXSID00357627

Synonyms:6662-59-5;4-[2-(4-chlorophenyl)ethenyl]-1-ethylpyridin-1-ium;DTXSID00357627;AKOS000678622

Suppliers and Price of 4-[2-(4-Chlorophenyl)ethenyl]-1-ethylpyridin-1-ium

Supply Marketing:

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

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Total 0 raw suppliers

Chemical Property of 4-[2-(4-Chlorophenyl)ethenyl]-1-ethylpyridin-1-ium

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:244.0893022
Heavy Atom Count:17
Complexity:235

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC[N+]1=CC=C(C=C1)C=CC2=CC=C(C=C2)Cl

Technology Process of 4-[2-(4-Chlorophenyl)ethenyl]-1-ethylpyridin-1-ium

There total 3 articles about 4-[2-(4-Chlorophenyl)ethenyl]-1-ethylpyridin-1-ium 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:

: 853-23-6
prasterone acetate

: 6662-59-5
3β-Chlor-17β-methylamino-androst-5-en-N-isopropyloxyacetat

Guidance literature:: Multi-step reaction with 3 steps

1: NaOMe

2: NaBH₄

3: Et₃N

With sodium tetrahydroborate; sodium methylate; triethylamine;
DOI:10.1016/0039-128X(66)90144-9

Reference yield:

: 17-Methylimino-androst-5-en-3β-ol

: 6662-59-5
3β-Chlor-17β-methylamino-androst-5-en-N-isopropyloxyacetat

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄

2: Et₃N

With sodium tetrahydroborate; triethylamine;
DOI:10.1016/0039-128X(66)90144-9