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2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride

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Name

2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride

EINECS N/A
CAS No. 91374-25-3 Density N/A
PSA 86.36000 LogP 4.21160
Solubility N/A Melting Point 188-192 °C
Formula C16H25ClN2O4 Boiling Point N/A
Molecular Weight 344.838 Flash Point N/A
Transport Information N/A Appearance N/A
Safety Risk Codes N/A
Molecular Structure Molecular Structure of 91374-25-3 (2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride) Hazard Symbols N/A
Synonyms

Benzeneaceticacid, 2-[2-(dipropylamino)ethyl]-6-nitro-, monohydrochloride (9CI);[2-Nitro-6-(2-dipropylaminoethyl)phenyl]acetic acid hydrochloride;benzeneacetic acid, 2-[2-(dipropylamino)ethyl]-6-nitro-, hydrochloride (1:1);{2-[2-(Dipropylamino)ethyl]-6-nitrophenyl}acetic acid hydrochloride (1:1);

Article Data 4

2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride Specification

The 2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride, with the CAS registry number 91374-25-3, has the systematic name of benzeneacetic acid, 2-[2-(dipropylamino)ethyl]-6-nitro-, hydrochloride (1:1). It belongs to the product categories of Pharmaceutical material and intermeidates. And the molecular formula of this chemical is C16H25ClN2O4.

Preparation of 2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride: This chemical can be prepared by 2-nitro-6-[2-(N,N-di-n-propylamino)ethyl]phenylpyruvic acid. The reaction will need reagents 2% aq. NaOH and 30% aq. H2O2. The reaction time is 1 hour with ambient temperature, and the yield is about 80%. 

2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride can be prepared by 2-nitro-6-[2-(N,N-di-n-propylamino)ethyl]phenylpyruvic acid

Uses of 2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride: It can be used to produce 4-[2-(di-n-propylamino)ethyl]-2(3H)-indolone. This reaction will need reagent H2, catalyset 5% Pd/C, and the solvent ethanol. The reaction time is 5 hours with the pressure of 2585.7Pa. 

2-[2-(Dipropylamino)ethyl]-6-nitrophenylacetic acid hydrochloride can be used to produce 4-[2-(di-n-propylamino)ethyl]-2(3H)-indolone

You can still convert the following datas into molecular structure:
(1)SMILES: CCCN(CCC)CCc1cccc(c1CC(=O)O)[N+](=O)[O-].Cl
(2)InChI: InChI=1/C16H24N2O4.ClH/c1-3-9-17(10-4-2)11-8-13-6-5-7-15(18(21)22)14(13)12-16(19)20;/h5-7H,3-4,8-12H2,1-2H3,(H,19,20);1H
(3)InChIKey: FPWCGNYEZSMQIY-UHFFFAOYAF

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