1-{[(chlorocarbonyl)oxy]methyl}-9H-fluorene-9-sulfonic acid

Base Information

• Chemical Name: 1-{[(chlorocarbonyl)oxy]methyl}-9H-fluorene-9-sulfonic acid
• CAS No.: 67827-06-9
• Molecular Formula: C15H11ClO5S
• Molecular Weight: 338.768
• DSSTox Substance ID: DTXSID30699663
• Mol file: 67827-06-9.mol

Synonyms:SCHEMBL1934600;DTXSID30699663;1-{[(chlorocarbonyl)oxy]methyl}-9H-fluorene-9-sulfonic acid

Chemical Property of 1-{[(chlorocarbonyl)oxy]methyl}-9H-fluorene-9-sulfonic acid

Chemical Property:

• PSA: 89.05000
• LogP: 4.50180
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 338.0015723
• Heavy Atom Count: 22
• Complexity: 529

Purity/Quality:

99% ^*data from raw suppliers

9-(2-SULFO)-FLUORENYLMETHYLOXYCARBONYL CHLORIDE 98.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(C3=C(C=CC=C23)COC(=O)Cl)S(=O)(=O)O

Technology Process of 1-{[(chlorocarbonyl)oxy]methyl}-9H-fluorene-9-sulfonic acid

There total 1 articles about 1-{[(chlorocarbonyl)oxy]methyl}-9H-fluorene-9-sulfonic acid 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:

(fluorenylmethoxy)carbonyl chloride (28920-43-6) → 2-sulfo-9-fluorenylmethoxycarbonyl chloride (67827-06-9)

Guidance literature:

With chlorosulfonic acid; In dichloromethane;

DOI:10.1021/jo00419a021

Reference yield: 73.0%

2-sulfo-9-fluorenylmethoxycarbonyl chloride (67827-06-9) + 6-amino-4-[(3-chlorophenyl)amino]quinazoline (153436-71-6) → C29H21ClN4O5S

Guidance literature:

With potassium acetate; In ethyl acetate; at 20 ℃; for 1152h;

upstream raw materials:

(fluorenylmethoxy)carbonyl chloride