2-(Diphenylmethanesulfinyl)ethan-1-amine

Base Information

Chemical Name:2-(Diphenylmethanesulfinyl)ethan-1-amine
CAS No.:90213-10-8
Molecular Formula:C15H17NOS
Molecular Weight:259.372
Hs Code.:
ChEMBL ID:CHEMBL3126737
DSSTox Substance ID:DTXSID20533284

Synonyms:CHEMBL3126737;90213-10-8;2-(Diphenylmethanesulfinyl)ethan-1-amine;SCHEMBL10953481;US9862679, Compound 5a;DTXSID20533284;SHMYXVVITSBKCM-UHFFFAOYSA-N;BDBM364412;2-(Benzhydrylsulfinyl)ethan-1-amine;BDBM50496378

Suppliers and Price of 2-(Diphenylmethanesulfinyl)ethan-1-amine

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-(Diphenylmethanesulfinyl)ethan-1-amine

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:259.10308534
Heavy Atom Count:18
Complexity:239

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC=C2)S(=O)CCN

Technology Process of 2-(Diphenylmethanesulfinyl)ethan-1-amine

There total 2 articles about 2-(Diphenylmethanesulfinyl)ethan-1-amine 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: 43.0%

: 15515-58-9
N-<2-(diphenylmethylthio)ethyl>amine hydrochloride

: 90213-10-8
2-(benzhydrylsulfinyl)ethan-1-amine

Guidance literature:: With sodium periodate; In ethanol; water; at 0 - 20 ℃; for 20h; Inert atmosphere;
DOI:10.1021/jm401754x

Reference yield:

: 91-01-0
1,1-Diphenylmethanol

: 90213-10-8
2-(benzhydrylsulfinyl)ethan-1-amine

Guidance literature:: Multi-step reaction with 2 steps

1: boron trifluoride diethyl etherate; acetic acid / 0.33 h / 90 - 95 °C

2: sodium periodate / ethanol; water / 20 h / 0 - 20 °C / Inert atmosphere

With sodium periodate; boron trifluoride diethyl etherate; acetic acid; In ethanol; water;
DOI:10.1021/jm401754x