N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide
CAS No.:120350-84-7
Molecular Formula:C₁₇H₂₂FNO₂S
Molecular Weight:323.432
Hs Code.:
DSSTox Substance ID:DTXSID501162103

Synonyms:DTXSID501162103;N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide;120350-84-7

Suppliers and Price of N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide

Supply Marketing:

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

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Chemical Property of N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:323.13552828
Heavy Atom Count:22
Complexity:534

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC23CC4CC(C2)CC(C4)(C3)F

Technology Process of N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide

There total 3 articles about N-(3-Fluorotricyclo[3.3.1.13,7]dec-1-yl)-4-methylbenzenesulfonamide 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: 71.2%

: 120350-83-6
3-fluoro-1-aminoadamantane hydrochloride

: 98-59-9
p-toluenesulfonyl chloride

: 120350-84-7
3-fluoro-1-(N-adamantyl)-p-toluenesulfonamide

Guidance literature:: With potassium hydroxide; In diethyl ether; Ambient temperature;

Reference yield:

: 6239-83-4
3-fluoro-1-adamantane carboxamide

: 120350-84-7
3-fluoro-1-(N-adamantyl)-p-toluenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 80.2 percent / 1.) clorox, 2.) HCl (gas) / 1.) reflux

2: 71.2 percent / KOH (aq.) / diethyl ether / Ambient temperature

With hydrogenchloride; potassium hydroxide; sodium hypochlorite; In diethyl ether;

Reference yield:

: 42711-75-1
3-hydroxyadamantane-1-carboxylic acid

: 120350-84-7
3-fluoro-1-(N-adamantyl)-p-toluenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) 1-(N,N-diethylamino)-1,1,2-trifluoro-2-chloroethane, 2.) NH₄OH / 2.) ether

2: 80.2 percent / 1.) clorox, 2.) HCl (gas) / 1.) reflux

3: 71.2 percent / KOH (aq.) / diethyl ether / Ambient temperature

With hydrogenchloride; N-(2-chloro-1,1,2-trifluoroethyl)diethylamine; potassium hydroxide; ammonium hydroxide; sodium hypochlorite; In diethyl ether;