Phenyl sulfamate

Base Information

• Chemical Name: Phenyl sulfamate
• CAS No.: 19792-91-7
• Molecular Formula: C6H7NO3S
• Molecular Weight: 173.192
• Hs Code.: 2935009090
• European Community (EC) Number: 803-089-1
• DSSTox Substance ID: DTXSID50452510
• Nikkaji Number: J1.517.788H
• Pharos Ligand ID: ZH8LTPPDAFHH
• ChEMBL ID: CHEMBL24259
• Mol file: 19792-91-7.mol

Synonyms:phenyl sulfamate;phenylsulfamate;19792-91-7;Sulfamic acid phenyl ester;CHEMBL24259;Sulfamic acid, phenyl ester;D0L4FM;MLS001106216;SCHEMBL605969;DTXSID50452510;XOIYZMDJFLKIEI-UHFFFAOYSA-N;HMS2205G22;HMS3328F04;BDBM50098106;AT24286;SMR000639519;HY-117293;CS-0065216;FT-0747338;EN300-1718964;Z1255360895

Chemical Property of Phenyl sulfamate

Chemical Property:

• PSA: 77.77000
• LogP: 2.05000
• XLogP3: 0.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 173.01466426
• Heavy Atom Count: 11
• Complexity: 200

Purity/Quality:

98.5% ^*data from raw suppliers

PHENYL SULFAMATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)OS(=O)(=O)N

Technology Process of Phenyl sulfamate

There total 13 articles about Phenyl sulfamate 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: 96.0%

(E)-phenyl(piperidin-1-ylmethylene)sulfamate → phenyl sulfamate (19792-91-7)

Guidance literature:

With hydrazine hydrate; In ethanol; at 20 ℃; for 2h;

DOI:10.1080/00397911.2017.1361999

Reference yield: 93.0%

(E)-phenyl((diethylamino)methylene)sulfamate → phenyl sulfamate (19792-91-7)

Guidance literature:

With hydrazine hydrate; In ethanol; at 20 ℃; for 1.5h;

DOI:10.1080/00397911.2017.1361999

Reference yield: 89.0%

(E)-phenyl((dimethylamino)methylene)sulfamate → phenyl sulfamate (19792-91-7)

Guidance literature:

With hydrazine hydrate; In ethanol; at 20 ℃; for 1h;

DOI:10.1080/00397911.2017.1361999

upstream raw materials:

isocyanate de phenoxysulfonyle

sulphamoyl chloride

phenol

phenoxysulfonyl azide

Downstream raw materials:

phenyl N,N-dimethylsulfamate

1-[(2-Methoxyphenoxy)methyl]-1,2-ethanediol bissulfamate (ester)

phenol

aminosulfonic acid