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5044-21-3

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5044-21-3 Usage

General Description

Ethyl 2,5-dimethylpyrrole-1-acetate, also known as 2,5-dimethyl-1-ethoxycarbonylpyrrole, is a chemical compound with the molecular formula C9H13NO2. It is classified as an ester and is commonly used as a flavoring agent in the food and beverage industry. It is often added to various products to impart a fruity, berry-like aroma and taste. Additionally, it is used as a fragrance ingredient in perfumes and personal care products. Ethyl 2,5-dimethylpyrrole-1-acetate is known for its sweet, fruity, and floral scent, and is carefully formulated and regulated to ensure it is safe for consumer use.

Check Digit Verification of cas no

The CAS Registry Mumber 5044-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,4 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5044-21:
(6*5)+(5*0)+(4*4)+(3*4)+(2*2)+(1*1)=63
63 % 10 = 3
So 5044-21-3 is a valid CAS Registry Number.

5044-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2,5-dimethylpyrrol-1-yl)acetate

1.2 Other means of identification

Product number -
Other names ETHYL2-(2,5-DIMETHYLPYRROLYL)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:5044-21-3 SDS

5044-21-3Relevant articles and documents

Synthesis method of 1-aminomethyl-1-cyclopropanol

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Paragraph 0033-0037, (2020/08/09)

The invention discloses a synthetic method of 1-aminomethyl-1-cyclopropanol. The synthetic method comprises the following steps: adding a compound C00 into an aqueous potassium carbonate solution to form a first solution; adding an aqueous solution of C01 into the first solution for a reaction; combining organic phases, carrying out cleaning with saline water, and performing drying, filtering andconcentrating to obtain a compound C02; dissolving the compound C02 in tetrahydrofuran to form a second solution; adding tetraisopropyl titanate into the second solution to form a third solution; adding an ethyl magnesium bromide solution into the third solution for a reaction; adding an aqueous ammonium chloride solution into the solution for a quenching reaction; combining organic layers to obtain a compound C03; dissolving the compound C03 into an absolute ethyl alcohol solution to form a fourth solution; adding a sodium hydroxide solution into the fourth solution; adding a hydroxylamine hydrochloride solution into the fourth solution to form a fifth solution; and adding a sodium hydroxide solution into the fifth solution until the pH value is 6-7, and carrying out distilling to removea water phase, thereby obtaining the product, i.e., 1-aminomethyl-1-cyclopropanol. In this way, palladium hydroxide is not used as a catalyst, and synthesis cost is reduced.

CRTH2 MODULATORS

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Page/Page column 46, (2011/06/28)

Modulators of CRTH2, particularly antagonists of CRTH2, that are useful for treating various disorders, including asthma and respiratory disorders are disclosed. The compounds fall within a genus described by formula I:

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