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169376-35-6

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  • BEST PRICE/ETHYL-2-PYRROLOYL-ACETATE CAS NO.169376-35-6

    Cas No: 169376-35-6

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169376-35-6 Usage

General Description

ETHYL-2-PYRROLOYL-ACETATE is a chemical compound with the molecular formula C8H11NO2. It is an ester with a pyrrole ring structure, and is commonly used as a flavoring and fragrance ingredient in the perfume and food industries. It has a sweet, fruity odor with floral and woody undertones, making it a popular choice for adding a pleasant fragrance to various products. ETHYL-2-PYRROLOYL-ACETATE is commonly found in perfumes, soaps, lotions, and other scented products, and is also used in the production of artificial fruit flavors. Additionally, it is used as a solvent and in the manufacturing of pharmaceuticals and other chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 169376-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169376-35:
(8*1)+(7*6)+(6*9)+(5*3)+(4*7)+(3*6)+(2*3)+(1*5)=176
176 % 10 = 6
So 169376-35-6 is a valid CAS Registry Number.

169376-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-oxo-3-(1H-pyrrol-2-yl)propanoate

1.2 Other means of identification

Product number -
Other names 3-oxo-3-pyrrol-2-yl-propionic acid ethyl ester

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:169376-35-6 SDS

169376-35-6Downstream Products

169376-35-6Relevant articles and documents

Bromide-Mediated C-H Bond Functionalization: Intermolecular Annulation of Phenylethanone Derivatives with Alkynes for the Synthesis of 1-Naphthols

Lu, Tao,Jiang, Ya-Ting,Ma, Feng-Ping,Tang, Zi-Jing,Kuang, Liu,Wang, Yu-Xuan,Wang, Bin

supporting information, p. 6344 - 6347 (2017/12/08)

Bromide-mediated intermolecular annulation of phenylethanone derivatives with alkynes has been developed, which allows for the regioselective formation of polysubstituted 1-naphthols. The usage of readily available bromine catalyst, broad substrate scope, and mild conditions make this protocol very practical. Mechanistic investigations reveal that the bromination of phenylethanone derivatives occurs to yield bromo-substituted intermediates, which react in situ with alkynes to furnish the desired 1-naphthols.

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