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Prop-2-yn-1-yl phenoxyacetate, also known as 2-propyn-1-yl phenoxyacetate, is an organic compound with the chemical formula C11H10O3. It is a derivative of phenoxyacetic acid, featuring a propargyl group (a three-carbon chain with a triple bond at one end) attached to the phenoxy group. prop-2-yn-1-yl phenoxyacetate is characterized by its unique structure, which includes a phenyl ring (a benzene ring) connected to an acetate group through an oxygen atom, and a propargyl group attached to the acetate. It is used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. Due to its reactivity and functional groups, prop-2-yn-1-yl phenoxyacetate can participate in a range of chemical transformations, making it a valuable intermediate in organic synthesis.

5423-30-3

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5423-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5423-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5423-30:
(6*5)+(5*4)+(4*2)+(3*3)+(2*3)+(1*0)=73
73 % 10 = 3
So 5423-30-3 is a valid CAS Registry Number.

5423-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-ynyl 2-phenoxyacetate

1.2 Other means of identification

Product number -
Other names prop-2-yn-1-yl phenoxyacetate

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:5423-30-3 SDS

5423-30-3Downstream Products

5423-30-3Relevant academic research and scientific papers

Exploration of click reaction for the synthesis of modified nucleosides as chitin synthase inhibitors

Chaudhary, Preeti M.,Chavan, Sayalee R.,Shirazi, Fazal,Razdan, Meenakshi,Nimkar, Prachi,Maybhate, Shailaja P.,Likhite, Anjali P.,Gonnade, Rajesh,Hazara, Braja G.,Deshpande, Mukund V.,Deshpande, Sunita R.

body text, p. 2433 - 2440 (2009/09/05)

Click reaction approach toward the synthesis of two sets of novel 1,2,3-triazolyl linked uridine derivatives 19a-19g and 21a-21g was achieved by Cu(I)-catalyzed 1,3-dipolar cycloaddition of 5′-azido-5′-deoxy-2′,3′-O-(1-methylethylidene)uridine (17) with p

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