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Ethyl-6-methylpyridine-2-acetate, a chemical compound with the molecular formula C11H13NO2, is a derivative of pyridine and acetate. It is characterized by its fruity, floral odor and is widely used as a flavoring agent or fragrance in various consumer products.

5552-83-0

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5552-83-0 Usage

Uses

Used in Perfumery and Cosmetics Industry:
Ethyl-6-methylpyridine-2-acetate is used as a fragrance ingredient for its pleasant, fruity, and floral scent, enhancing the olfactory appeal of perfumes and cosmetics.
Used in Food and Beverage Industry:
In the food and beverage sector, Ethyl-6-methylpyridine-2-acetate is used as a flavoring agent to impart a desirable aroma to products, improving their sensory attributes.
Used in Pharmaceutical Industry:
Ethyl-6-methylpyridine-2-acetate is utilized in the manufacturing of pharmaceuticals, contributing to the development of medications with improved scent profiles, which can enhance patient compliance.
Used in Pesticide Industry:
Ethyl-6-methylpyridine-2-acetate also finds application in the production of pesticides, where its unique properties may contribute to the effectiveness or appeal of these agricultural chemicals.
Safety Precautions:
Due to its potential hazards if not properly managed, Ethyl-6-methylpyridine-2-acetate should be handled and used with caution to ensure safety in all applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5552-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5552-83:
(6*5)+(5*5)+(4*5)+(3*2)+(2*8)+(1*3)=100
100 % 10 = 0
So 5552-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-3-13-10(12)7-9-6-4-5-8(2)11-9/h4-6H,3,7H2,1-2H3

5552-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-(6-methylpyridin-2-yl)acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-(6-methylpyridin-2-yl)acetate

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:5552-83-0 SDS

5552-83-0Relevant academic research and scientific papers

PYRIDAZINE COMPOUND AND USE THEREOF

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Page/Page column 38, (2008/12/07)

A pyridazine compound of the formula: has an excellent plant disease controlling effect.

Syntheses and structure-activity relationship studies of piperidine-substituted quinolones as nonpeptide gonadotropin releasing hormone antagonists

Jiang, Jinlong,DeVita, Robert J.,Goulet, Mark T.,Wyvratt, Matthew J.,Lo, Jane-L.,Ren, Ning,Yudkovitz, Joel B.,Cui, Jisong,Yang, Yi T.,Cheng, Kang,Rohrer, Susan P.

, p. 1795 - 1798 (2007/10/03)

Syntheses and structure-activity relationships of piperidine-substituted quinolones as nonpeptide gonadotropin releasing hormone antagonists are described. Some of substituents on the piperidine ring that were investigated included a fused phenyl group, a

Reductive Amination of Ethynylpyridines with Sodium Cyanoborohydride

Sakamoto, Takao,Nagata, Hideo,Kondo, Yoshinori,Sato, Kaori,Yamanaka, Hiroshi

, p. 4866 - 4872 (2007/10/02)

In order to investigate the structure-activity relationship of betahistine derivatives, a general synthesis of methylated 2-(2-methylaminoethyl)pyridines was developed based on the addition of methylamine hydrochloride to methylated 2-ethynylpyridines under reductive conditions.In addition, the scope and limitations of the reductive addition were briefly examined.For example, the reaction proceeded smoothly with p-nitrophenylacetylene, whereas phenylacetylene itself did not react with methylamine.Keywords - ethynylpyridine; sodium cyanoborohydride; reductive amination; betahistine; palladium-catalyzed reaction; ethyl pyridineacetate; 2-(2-pyridyl)ethylamine

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