Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate

Base Information

Chemical Name:Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate
CAS No.:72353-30-1
Molecular Formula:C₁₈H₁₈O₂S
Molecular Weight:298.406
Hs Code.:
DSSTox Substance ID:DTXSID80993148
Mol file:72353-30-1.mol

Synonyms:Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate;72353-30-1;(1-(2-Fluorenyl)-aethylmercapto)essigsaeuremethyl ester [German];Acetic acid, ((1-(9H-fluoren-2-yl)ethyl)thio)-, methyl ester, (+-)-;(1-(2-Fluorenyl)-aethylmercapto)essigsaeuremethyl ester;C18H18O2S;DTXSID80993148;Methyl {[1-(9H-fluoren-2-yl)ethyl]sulfanyl}acetate

Suppliers and Price of Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate

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)-AETHYLMERCAPTO)ESSIGSAEUREMETHYL ESTER [GERMAN] 95.00%
5MG
$ 497.52

Total 1 raw suppliers

Chemical Property of Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate

Chemical Property:

Vapor Pressure:1.17E-07mmHg at 25°C
Boiling Point:431.8°C at 760 mmHg
Flash Point:208.5°C
PSA：51.60000
Density:1.199g/cm³
LogP:4.22500
XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:298.10275099
Heavy Atom Count:21
Complexity:370

Purity/Quality:: (1-(2-FLUORENYL)-AETHYLMERCAPTO)ESSIGSAEUREMETHYL ESTER [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)SCC(=O)OC

Technology Process of Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate

There total 8 articles about Methyl (+-)-((1-(9H-fluoren-2-yl)ethyl)thio)acetate 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

: 72353-30-1,72353-36-7,72353-39-0
[1-(9H-Fluoren-2-yl)-ethylsulfanyl]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / chloroform; toluene

2: thionyl chloride

With thionyl chloride; trichlorophosphate; In chloroform; toluene;

Reference yield:

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

: 72353-30-1,72353-36-7,72353-39-0
[1-(9H-Fluoren-2-yl)-ethylsulfanyl]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

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

2: thionyl chloride

With thionyl chloride;

Reference yield:

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

: 72353-30-1,72353-36-7,72353-39-0
[1-(9H-Fluoren-2-yl)-ethylsulfanyl]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / methanol

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

3: thionyl chloride

With sodium hydroxide; thionyl chloride; In methanol;