((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid

Base Information

Chemical Name:((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid
CAS No.:72322-15-7
Molecular Formula:C₁₇H₁₆O₃S
Molecular Weight:300.378
Hs Code.:
DSSTox Substance ID:DTXSID50993115
Mol file:72322-15-7.mol

Synonyms:72322-15-7;((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid;(1-(2-Fluorenyl)-aethylsulfinyl)essigsaeure [German];Acetic acid, ((1-(9H-fluoren-2-yl)ethyl)sulfinyl)-;(1-(2-Fluorenyl)-aethylsulfinyl)essigsaeure;DTXSID50993115;2-((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)aceticacid;2-((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid;[1-(9H-FLUOREN-2-YL)ETHANESULFINYL]ACETIC ACID

Suppliers and Price of ((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
(1-(2-FLUORENYL)-AETHYLSULFINYL)ESSIGSAEURE [GERMAN] 95.00%
5MG
$ 499.39

Total 0 raw suppliers

Chemical Property of ((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid

Chemical Property:

Vapor Pressure:9.97E-15mmHg at 25°C
Boiling Point:589.2°C at 760 mmHg
Flash Point:310.1°C
PSA：73.58000
Density:1.371g/cm³
LogP:4.01780
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:300.08201554
Heavy Atom Count:21
Complexity:422

Purity/Quality:: (1-(2-FLUORENYL)-AETHYLSULFINYL)ESSIGSAEURE [GERMAN] 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC2=C(C=C1)C3=CC=CC=C3C2)S(=O)CC(=O)O

Technology Process of ((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic acid

There total 8 articles about ((1-(9H-Fluoren-2-yl)ethyl)sulfinyl)acetic 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:

: 20371-86-2
1-(9H-fluoren-2-yl)ethan-1-ol

: 72322-15-7
[1-(9H-Fluoren-2-yl)-ethanesulfinyl]-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / chloroform; toluene

2: dihydrogen peroxide

With dihydrogen peroxide; trichlorophosphate; In chloroform; toluene;

Reference yield:

: 72322-10-2
1-(9H-Fluoren-2-yl)-ethanethiol

: 72322-15-7
[1-(9H-Fluoren-2-yl)-ethanesulfinyl]-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: (i) K₂CO₃, DMSO, (ii) /BRN= 605438/

2: dihydrogen peroxide

With dihydrogen peroxide;

Reference yield:

: Diaminomethylene-[1-(9H-fluoren-2-yl)-ethyl]-sulfonium; chloride

: 72322-15-7
[1-(9H-Fluoren-2-yl)-ethanesulfinyl]-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / methanol

2: (i) K₂CO₃, DMSO, (ii) /BRN= 605438/

3: dihydrogen peroxide

With sodium hydroxide; dihydrogen peroxide; In methanol;