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3-amino-5-phenyldihydrofuran-2(3H)-one is a heterocyclic organic compound characterized by a dihydrofuran ring, which is a partially saturated furan ring. The molecule features an amino group at the 3-position and a phenyl group at the 5-position. 3-amino-5-phenyldihydrofuran-2(3H)-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can act as a building block for the creation of more complex molecules, particularly those with potential biological activity. The compound's properties, such as its ability to form hydrogen bonds and its aromatic character, make it a valuable intermediate in organic synthesis.

3790-22-5

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3790-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3790-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3790-22:
(6*3)+(5*7)+(4*9)+(3*0)+(2*2)+(1*2)=95
95 % 10 = 5
So 3790-22-5 is a valid CAS Registry Number.

3790-22-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-5-phenyloxolan-2-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Amino-5-phenyl-dihydro-furan-2-on,Hydrochlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3790-22-5 SDS

3790-22-5Downstream Products

3790-22-5Relevant academic research and scientific papers

Synthesis of enantiomerically pure 2-alkyl 1-amino cyclopropane-1-carboxylic acid

Calmes, Monique,Daunis, Jacques,Escale, Francoise

, p. 395 - 396 (2007/10/03)

Asymmetric synthesis of 1-amino 2-alkyl cyclopropane carboxylic acids using (1R,2R,5R)-2-hydroxy pinan-3-one as the chiral auxiliary and Corey's ylide as reagent is described.

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