dimethyl(2-phenoxyethyl)amine

  • CAS：13468-02-5
  • purity：99%
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Good factory supply good dimethyl(2-phenoxyethyl)amine 13468-02-5 We supply high quality dimethyl(2-phenoxyethyl)amine (CAS 13468-02-5), in stock, factory directly supply to clients, lower prices, more competitiveness.

What is the dimethyl(2-phenoxyethyl)amine ?

dimethyl(2-phenoxyethyl)amine is , while it's Molecular Formula is C10H15 N O. N,N-Dimethyl-2-phenoxyethanamine is useful for the preparation of histone deacetylase inhibitors.

What is the CAS number for dimethyl(2-phenoxyethyl)amine ?

The CAS number of dimethyl(2-phenoxyethyl)amine is 13468-02-5.

More information of dimethyl(2-phenoxyethyl)amine 13468-02-5 are:

Synonyms

Ethylamine,N,N-dimethyl-2-phenoxy- (7CI,8CI); (2-Dimethylaminoethoxy)benzene;2-(Dimethylamino)ethyl phenyl ether; 2-(N,N-Dimethylamino)ethyl phenyl ether;Dimethyl(2-phenoxyethyl)amine; N,N-Dimethyl-2-phenoxyethylamine

CAS?Number

13468-02-5

Molecular Formula

C10H15 N O

Molecular Weight

165.235

Density

0.97g/cm3

Melting Point

163-164 °C(Solv: isopropanol (67-63-0))

Boiling Point

231.5°Cat760mmHg

Flash Point

67.1°C

HS CODE

2922299090

PSA

12.47000

LogP

1.62700

Pka

8.80±0.28(Predicted)

What is dimethyl(2-phenoxyethyl)amine (13468-02-5) used for?

Dimethyl(2-phenoxyethyl)amine, also known as N,N-Dimethyl-2-phenoxyethanamine, is an organic compound with the molecular formula C10H15NO. It is a derivative of phenoxyethanamine, featuring two methyl groups attached to the nitrogen atom. dimethyl(2-phenoxyethyl)amine is known for its potential applications in the pharmaceutical and chemical industries due to its unique structural properties.

InChI:InChI=1/C10H15NO/c1-11(2)8-9-12-10-6-4-3-5-7-10/h3-7H,8-9H2,1-2H3

Articles related to dimethyl(2-phenoxyethyl)amine:

Article

Source

The solid state structures of ortho-lithio-β-(N,N-dimethylamino)ethoxybenzene and the corresponding sodium compound: A new type of organolithium tetramer and a first example of an organosodium hexamer

Den Besten, Remco,Lakin, Miles T.,Veldman, Nora,Spek, Anthony L.,Brandsma, Lambert

, p. 191 - 196 (1996)

Mustard Carbonate Analogues as Sustainable Reagents for the Aminoalkylation of Phenols

Annatelli, Mattia,Trapasso, Giacomo,Salaris, Claudio,Salata, Cristiano,Castellano, Sabrina,Aricò, Fabio

supporting information, p. 3459 - 3464 (2021/05/24)

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