3696-12-6 Usage
Description
(4-Hydroxy-3-methoxybenzylidene)malononitrile, also known as HMBM, is an organic compound that belongs to the class of malononitriles. It is recognized for its unique molecular structure and versatile reactivity in organic chemistry, which allows it to participate in a range of reactions such as Michael additions and Knoevenagel condensations. HMBM also exhibits photochromic and thermochromic properties, making it a compound of interest for the development of photoresponsive materials and potential applications in optical data storage and display devices. Its pale yellow color and distinctive characteristics have garnered attention in chemical research and development.
Uses
Used in Organic Chemistry:
(4-Hydroxy-3-methoxybenzylidene)malononitrile is used as a reactive intermediate for various organic synthesis processes due to its ability to undergo Michael additions and Knoevenagel condensations, which are crucial for creating a wide array of chemical products.
Used in Photoresponsive Materials:
(4-Hydroxy-3-methoxybenzylidene)malononitrile is used as a key component in the development of photoresponsive materials because of its photochromic and thermochromic properties, which allow for changes in the compound's structure upon exposure to light or changes in temperature.
Used in Optical Data Storage and Display Devices:
(4-Hydroxy-3-methoxybenzylidene)malononitrile is used as a material in the research and development of optical data storage and display devices, leveraging its unique photoresponsive characteristics to enhance the performance and functionality of these technologies.
Used in Chemical Research and Development:
(4-Hydroxy-3-methoxybenzylidene)malononitrile serves as a valuable target for chemical research and development due to its distinctive molecular structure and the potential for creating new compounds and materials with novel properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3696-12-6 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 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3696-12:
(6*3)+(5*6)+(4*9)+(3*6)+(2*1)+(1*2)=106
106 % 10 = 6
So 3696-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2O2/c1-15-11-5-8(2-3-10(11)14)4-9(6-12)7-13/h2-5,14H,1H3
3696-12-6Relevant articles and documents
Structural characterization of monomers for non-linear optical polymers. X-ray analysis and molecular mechanics calculations of 2-(4-methacryloxy-3- methoxyphenyl)-1,1-dicyanoethylene, 2-(3-methacryloxy-4-methoxyphenyl)-1,1- dicyanoethylene, and 2-(2-meth
Nesterov,Deng,Timofeeva,Antipin, M.Yu.,Clark,Frazier,Penn
, p. 309 - 318 (2000)
The results of molecular mechanics calculations, hyperpolarizabilities calculations, synthesis, and X-ray analysis of three monomers for non-linear optical polymers are presented. All monomers are derivatives of dicyanovinylbenzene with methoxy and methac
Ferrocene-Functionalized Dithiocarbamate Zinc(II) Complexes as Efficient Bifunctional Catalysts for the One-Pot Synthesis of Chromene and Imidazopyrimidine Derivatives via Knoevenagel Condensation Reaction
Anamika,Drew, Michael G. B.,Kumar, Kamlesh,Singh, Nanhai,Yadav, Chote Lal
, p. 6446 - 6462 (2021/05/31)
Four new mononuclear/coordination polymeric (CP) zinc(II) complexes (1-4) of ferrocenyl/pyridyl-functionalized dithiocarbamate ligands, N-ferrocenylmethyl-N-butyl dithiocarbamate (L1), N-ferrocenylmethyl-N-ethylmorpholine dithiocarbamate (L2), N-ferroceny
LQFM184: A Novel Wide Ultraviolet Radiation Range Absorber Compound
Vinhal, Daniela C.,Ivan de ávila, Renato,Rodrigues, Thaisangela L.,Silva, Andressa K.,Moreira, Larissa C.,Valadares, Marize C.,Luzin, Rangel M.,Li?o, Luciano M.,Gil, Eric de S.,Vaz, Boniek G.,Assis, Rogério J.,Gon?alves, Pablo J.,Isaac, Vera,da Cunha, Luiz C.,Menegatti, Ricardo
, p. 360 - 371 (2020/12/04)
The use of sunscreen has become an indispensable daily routine since UV radiation is a critical environmental stress factors for human skin. This study focused on the design, synthesis, thermal/chemical stability and efficacy/safety evaluations of a new h