N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine

Base Information

Chemical Name:N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine
CAS No.:89478-93-3
Molecular Formula:C₁₂H₁₆BrNO₂S
Molecular Weight:318.235
Hs Code.:
DSSTox Substance ID:DTXSID20527269

Synonyms:89478-93-3;DTXSID20527269;N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine

Suppliers and Price of N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:317.00851
Heavy Atom Count:17
Complexity:329

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)C(CNCC=C)Br

Technology Process of N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine

There total 3 articles about N-[2-Bromo-2-(4-methylbenzene-1-sulfonyl)ethyl]prop-2-en-1-amine 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: 86.0%

: 89478-86-4
1-bromovinyl p-tolyl sulphone

: 107-11-9,30551-89-4
1-amino-2-propene

: 89478-93-3
2-allylamino-1-bromo-1-p-tolylsulphonylethane

Guidance literature:: In tetrahydrofuran; for 3.5h; Ambient temperature;

Reference yield:

: 5535-52-4
tolyl vinyl sulfone

: 89478-93-3
2-allylamino-1-bromo-1-p-tolylsulphonylethane

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / bromine / CCl₄ / 24 h / Ambient temperature

2: 70 percent / triethylamine / CH₂Cl₂ / 3.5 h

3: 86 percent / tetrahydrofuran / 3.5 h / Ambient temperature

With bromine; triethylamine; In tetrahydrofuran; tetrachloromethane; dichloromethane;

Reference yield:

: 59336-76-4
1,2-dibromo-1-p-tolylsulphonylethane

: 89478-93-3
2-allylamino-1-bromo-1-p-tolylsulphonylethane

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / triethylamine / CH₂Cl₂ / 3.5 h

2: 86 percent / tetrahydrofuran / 3.5 h / Ambient temperature

With triethylamine; In tetrahydrofuran; dichloromethane;