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13220-24-1

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13220-24-1 Usage

General Description

ETHYL 3-((2-ETHOXY-2-OXOETHYL)(METHYL) AMINO)PROPANOATE is a chemical compound with the molecular formula C10H19NO4. It is a ester formed by the condensation of ethyl 3-amino propionate and ethyl oxoacetate and commonly used as a flavoring agent in the food industry. ETHYL 3-((2-ETHOXY-2-OXOETHYL)(METHYL) AMINO)PROPANOATE has a fruity and sweet aroma and is used to enhance the flavor of various food and beverage products. It is also used in the production of perfumes and pharmaceuticals due to its pleasant smell and potential therapeutic properties. However, it is important to handle and use this chemical compound with caution, as it may present hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 13220-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13220-24:
(7*1)+(6*3)+(5*2)+(4*2)+(3*0)+(2*2)+(1*4)=51
51 % 10 = 1
So 13220-24-1 is a valid CAS Registry Number.

13220-24-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[(2-ethoxy-2-oxoethyl)-methylamino]propanoate

1.2 Other means of identification

Product number -
Other names <2-Ethoxycarbonyl-ethyl>-ethoxycarbonylmethyl-methylamin

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:13220-24-1 SDS

13220-24-1Downstream Products

13220-24-1Relevant articles and documents

Chiral arylpyrrolidinols: Preparation and biological profile

Collina, Simona,Rossi, Daniela,Loddo, Guya,Barbieri, Annalisa,Lanza, Enrica,Linati, Laura,Alcaro, Stefano,Gallelli, Andrea,Azzolina, Ornella

, p. 3117 - 3126 (2005)

The preparation and biological evaluation of a new class of arylpyrrolidinols is reported. The antinociceptive activity was evaluated in vivo with the hot plate test (HPT) and formalin test (FT), excluding any involvement on motor coordination with the rota-rod test (RRT). The nociceptive behavior in the late phase of FT (representative of chronic pain) suggests an involvement of the antiinflammatory process and it is clearly influenced by the stereochemical features, being the eutomer of phenylpyrrolidinols, the (2R,3S) enantiomer. Despite this, a specific mechanism of action is not yet clarified.

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