LP4Ckg54SR

Base Information

• Chemical Name: LP4Ckg54SR
• CAS No.: 60548-64-3
• Molecular Formula: C7H18N2O6S2
• Molecular Weight: 290.3576
• UNII: LP4CKG54SR
• ChEMBL ID: CHEMBL353458
• Nikkaji Number: J90.613A
• Wikidata: Q107845306
• Mol file: 60548-64-3.mol

Synonyms:LP4CKG54SR;CHEMBL353458;SCHEMBL11593381;QJQKZZCQOQXBQF-UHFFFAOYSA-N;(2,4-dimethyl-1-sulfamoyloxypentan-3-yl)sulfamate;2-Methyl-2-propyl-1,3-bis-O-sulfamyl-1,3-propanediol;Sulfamic acid, 2-methyl-2-propyl-1,3-propanediyl ester;2-methyl-1-(sulfamoyloxy)-2-[(sulfamoyloxy)methyl]pentane

Chemical Property of LP4Ckg54SR

Chemical Property:

• Vapor Pressure: 1.07E-08mmHg at 25°C
• Boiling Point: 461.4°Cat760mmHg
• Flash Point: 232.9°C
• Density: 1.4g/cm³
• XLogP3: -0.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 8
• Exact Mass: 290.06062865
• Heavy Atom Count: 17
• Complexity: 382

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC(C)(COS(=O)(=O)N)COS(=O)(=O)N

Technology Process of LP4Ckg54SR

There total 2 articles about LP4Ckg54SR 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:

2-methyl-2-propyl-1,3-propanediol (78-26-2) → Sulfamic acid 2-methyl-2-sulfamoyloxymethyl-pentyl ester (60548-64-3)

Guidance literature:

With sulphamoyl chloride; sodium hydride; Yield given. Multistep reaction; 1.) 1,2-dimethoxyethane, RT, 2 h, 2.) 1,2-dimethoxyethane, 4 deg C, 24 h;

DOI:10.1021/jm00139a029

Reference yield:

→ Sulfamic acid 2-methyl-2-sulfamoyloxymethyl-pentyl ester (60548-64-3)

Guidance literature:

Diol, Chlorsulfonamid;

upstream raw materials:

2-methyl-2-propyl-1,3-propanediol