3695-89-4 Usage
Description
(Z)-2-cyano-3-(4-hydroxyphenyl)acrylamide, a chemical compound with the molecular formula C11H8N2O2, is a derivative of acrylamide featuring a nitrile group and a hydroxyphenyl group. This yellow solid has a molecular weight of 204.19 g/mol and is recognized for its role in the synthesis of various organic compounds. Its structural attributes also make it a valuable building block in the production of pharmaceuticals and agrochemicals, with potential applications extending to materials science and biotechnology.
Uses
Used in Pharmaceutical Industry:
(Z)-2-cyano-3-(4-hydroxyphenyl)acrylamide is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure, which can be manipulated to create a range of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, (Z)-2-cyano-3-(4-hydroxyphenyl)acrylamide is used as a starting material for the development of new agrochemicals, potentially contributing to the creation of more effective pesticides or other agricultural products.
Used in Materials Science:
(Z)-2-cyano-3-(4-hydroxyphenyl)acrylamide is used as a component in the research and development of novel materials, possibly due to its ability to form complexes or its potential to be integrated into polymer systems.
Used in Biotechnology:
Within the biotechnology field, (Z)-2-cyano-3-(4-hydroxyphenyl)acrylamide may be utilized in the design of bioactive molecules or for the development of new biological tools, taking advantage of its reactive functional groups and structural diversity.
Check Digit Verification of cas no
The CAS Registry Mumber 3695-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3695-89:
(6*3)+(5*6)+(4*9)+(3*5)+(2*8)+(1*9)=124
124 % 10 = 4
So 3695-89-4 is a valid CAS Registry Number.
3695-89-4Relevant articles and documents
Triflic acid-catalyzed metal-free synthesis of (: E)-2-cyanoacrylamides and 3-substituted azetidine-2,4-diones
Rupanwar, Bapurao D.,Chavan, Santosh S.,Shelke, Anil M.,Suryavanshi, Gurunath M.
supporting information, p. 6433 - 6440 (2018/04/23)
A TfOH-catalyzed highly efficient synthesis of biologically active (E)-2-cyanoacrylamides and 3-substituted azetidine-2,4-diones has been reported with 64-94% yields under metal-free conditions. The reaction proceeds through sequential Knoevenagel condens
Regiospecific Mno2 catalyzed hydration of phenylmethylene malononitriles to cyanophenylacrylamides by oximes
Rauf, Abdul,Awan, Faisal Saleem,Mumtaz, Saira,Sharif, Ahsan,Ahmed, Ejaz,Arshad, Muhammad,Kausar, Farzana,Yasmin, Ghazala,Qureshi, Ashfaq Mahmood
experimental part, p. 728 - 731 (2012/08/07)
A novel and convenient method for the regiospecific hydration of phenylmethylene malononitriles to cyanoacrylamides was developed; Scope of the method and reaction conditions were optimized extensively, the method was found to be extremely successful in h
Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield
Kaupp, Gerd,Naimi-Jamal, M. Reza,Schmeyers, Jens
, p. 3753 - 3760 (2007/10/03)
Numerous Knoevenagel condensations of solid or liquid aromatic aldehydes are performed with four barbituric acids, Meldrum's acid, dimedone, cyanoacetamide, malodinitrile and methyl cyanoacetate in stoichiometric mixtures of the solids or of stoichiometri
