13234-71-4 Usage
Description
1-Naphthaleneacetic acid, a-cyano-, ethyl ester, also known as Ethyl 2-Cyano-2-(naphthalen-1-yl)acetate, is an organic compound derived from naphthalene and acetic acid. It is characterized by its unique chemical structure, which includes a naphthalene ring and a cyano group attached to an ethyl ester. 1-Naphthaleneacetic acid, a-cyano-, ethyl ester exhibits properties that make it suitable for various applications in different industries.
Uses
Used in Polymer Industry:
1-Naphthaleneacetic acid, a-cyano-, ethyl ester is used as a catalyst for the crosslinking of polyesters with styrene. Its unique chemical structure allows it to facilitate the formation of crosslinks between polyester and styrene molecules, resulting in improved mechanical properties and enhanced performance of the final polymer product.
The use of this compound as a catalyst in the polymer industry is particularly beneficial for the production of materials with specific properties, such as increased strength, durability, and resistance to environmental factors. By incorporating 1-Naphthaleneacetic acid, a-cyano-, ethyl ester into the polymerization process, manufacturers can create tailored polymers for various applications, including automotive components, packaging materials, and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 13234-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13234-71:
(7*1)+(6*3)+(5*2)+(4*3)+(3*4)+(2*7)+(1*1)=74
74 % 10 = 4
So 13234-71-4 is a valid CAS Registry Number.
13234-71-4Relevant articles and documents
Phosphine-catalyzed regioselective Michael addition to allenoates
Gandi, Vasudeva Rao,Lu, Yixin
supporting information, p. 16188 - 16190 (2015/11/10)
The first phosphine catalysed Michael addition of arylcyanoacetates to allenoates has been developed, and the β-selective products with a quaternary center were obtained in excellent yields. This unusual regioselectivity may open new opportunities to acce
A General Method for the Direct α-Arylation of Nitriles with Aryl Chlorides
You, Jingsong,Verkade, John G.
, p. 5051 - 5053 (2007/10/03)
The long-standing challenge of developing a general method for the title methodology is met for a broad range of aryl chlorides through the use of bicyclic P(iBuNCH2CH2)3N (1) as a bulky electron-rich ligand for palladium (see scheme, dba = dibenzylideneacetone).
Palladium-catalyzed arylation of ethyl cyanoacetate. Fluorescence resonance energy transfer as a tool for reaction discovery [21]
Stauffer,Beare,Stambuli,Hartwig
, p. 4641 - 4642 (2007/10/03)
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