N-(3-hydroxyphenyl)methanesulfonamide

Base Information

• Chemical Name: N-(3-hydroxyphenyl)methanesulfonamide
• CAS No.: 71290-40-9
• Molecular Formula: C₇H₉NO₃S
• Molecular Weight: 187.219
• Hs Code.: 2935909099
• European Community (EC) Number: 836-359-2
• Mol file: 71290-40-9.mol

Synonyms:N-(3-hydroxyphenyl)methanesulfonamide;71290-40-9;SCHEMBL9307026;DJQWZMOQUBMZGR-UHFFFAOYSA-N;MFCD04151187;AKOS008944057;MB03366;BS-29433;EN300-36770;Z45637535

Chemical Property of N-(3-hydroxyphenyl)methanesulfonamide

Chemical Property:

• Melting Point: 96-96.5 °C
• Boiling Point: 354.4±44.0 °C(Predicted)
• PKA: 8.28±0.10(Predicted)
• Density: 1.458±0.06 g/cm3(Predicted)
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 187.03031432
• Heavy Atom Count: 12
• Complexity: 232

Purity/Quality:

99% ^*data from raw suppliers

N-(3-hydroxyphenyl)methanesulfonamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CS(=O)(=O)NC1=CC(=CC=C1)O

Technology Process of N-(3-hydroxyphenyl)methanesulfonamide

There total 1 articles about N-(3-hydroxyphenyl)methanesulfonamide 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:

methanesulfonyl chloride (124-63-0) + m-Hydroxyaniline (591-27-5) → N-(3-hydroxyphenyl)methanesulfonamide (71290-40-9)

Guidance literature:

With pyridine; at 10 - 20 ℃; for 18h;

Reference yield: 89.0%

N-(3-hydroxyphenyl)methanesulfonamide (71290-40-9) + 2,4,6-trimethoxybenzaldehyde (830-79-5) → C17H21NO6S (1041367-63-8)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; at 20 ℃; for 4h;

DOI:10.1016/j.bmcl.2007.11.124

Reference yield: 18.0%

N-(3-hydroxyphenyl)methanesulfonamide (71290-40-9) + 2-(chloromethyl)-3-(phenylethynyl)imidazo[1,2-a]pyridine → N-(3-((3-(phenylethynyl)imidazo[1,2-a]pyridin-2-yl)methoxy)phenyl)methanesulfonamide

Guidance literature:

With caesium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 3h;

upstream raw materials:

methanesulfonyl chloride

m-Hydroxyaniline

Downstream raw materials:

C₁₇H₂₁NO₆S

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