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2-(2-oxo-2H-chromen-3-yl)ethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7151-73-7

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7151-73-7 Usage

Derived from

Chromene and acetic acid

Type of compound

Ester

Uses

Flavor and fragrance ingredient in perfumes, soaps, and personal care products

Odor

Sweet, floral

Antioxidant and antimicrobial properties

Potentially valuable in food and pharmaceutical applications

Used in

Organic synthesis and chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 7151-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7151-73:
(6*7)+(5*1)+(4*5)+(3*1)+(2*7)+(1*3)=87
87 % 10 = 7
So 7151-73-7 is a valid CAS Registry Number.

7151-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-oxochromen-3-yl)ethyl acetate

1.2 Other means of identification

Product number -
Other names -

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:7151-73-7 SDS

7151-73-7Downstream Products

7151-73-7Relevant academic research and scientific papers

Zn(II)-Catalyzed One-Pot Synthesis of Coumarins from Ynamides and Salicylaldehydes

Yoo, Huen Ji,Youn, So Won

, p. 3422 - 3426 (2019)

A highly efficient and straightforward synthesis of diversely substituted coumarins from ynamides and salicylaldehydes in the presence of Zn(II) catalyst has been developed. The sulfonamide moiety of ynamides was successfully recycled in this process, serving as an effective traceless directing group for high regioselectivity in the bond-forming event. The advantages of this protocol are good functional group tolerance, broad substrate scope, simple and high-yielding reaction, recovery/reuse of the sulfonamides, low catalyst loading of inexpensive catalyst, and, by these merits, a more cost-effective and greener process.

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