18167-91-4 Usage
Description
2-(2-Methoxyphenoxy)acetaldehyde, with the CAS number 18167-91-4, is an organic compound characterized by its off-white solid appearance. It is primarily utilized in various organic synthesis processes due to its unique chemical properties.
Uses
Used in Organic Synthesis:
2-(2-Methoxyphenoxy)acetaldehyde is used as a key intermediate in the synthesis of various organic compounds for different applications. Its chemical structure allows it to participate in a range of reactions, making it a versatile building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(2-Methoxyphenoxy)acetaldehyde is used as a starting material for the development of new drugs. Its unique structure can be modified to create molecules with specific therapeutic properties, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
2-(2-Methoxyphenoxy)acetaldehyde also finds application in the agrochemical sector, where it is used in the synthesis of active ingredients for pesticides and other crop protection products. Its role in creating effective and targeted agrochemicals helps ensure the sustainability and productivity of agricultural practices.
Used in Specialty Chemicals:
Furthermore, 2-(2-Methoxyphenoxy)acetaldehyde is employed in the production of specialty chemicals, which are used in a wide range of industries, including cosmetics, fragrances, and dyes. Its ability to form complex molecules with specific properties makes it an essential component in the development of innovative and high-quality specialty products.
Check Digit Verification of cas no
The CAS Registry Mumber 18167-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,6 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18167-91:
(7*1)+(6*8)+(5*1)+(4*6)+(3*7)+(2*9)+(1*1)=124
124 % 10 = 4
So 18167-91-4 is a valid CAS Registry Number.
18167-91-4Relevant articles and documents
GC–MS study of thermochemical conversion of guaifenesin in the presence of 1-butyl-3-methylimidazolium-based ionic liquids
Hamid, Sharifah Bee Abd,Khaligh, Nader Ghaffari,Sharifi, Mahdieh,Johari, Suzaimi
, p. 4007 - 4021 (2017)
Thermochemical conversion of guaifenesin was performed in the presence of 1-butyl-3-methylimidazolium tetrafluoroborate [BMIM][BF4] ionic liquid at 80?°C within 2?h. After evaluating the effect of different parameters, such as protic and nonpro
Ruthenium-Catalyzed C-C bond cleavage in lignin model substrates
Vom Stein, Thorsten,Den Hartog, Tim,Buendia, Julien,Stoychev, Spas,Mottweiler, Jakob,Bolm, Carsten,Klankermayer, Jürgen,Leitner, Walter
supporting information, p. 5859 - 5863 (2015/05/13)
Ruthenium-triphos complexes exhibited unprecedented catalytic activity and selectivity in the redox-neutral C-C bond cleavage of the β-O-4 lignin linkage of 1,3-dilignol model compounds. A mechanistic pathway involving a dehydrogenation-initiated retro-aldol reaction for the C-C bond cleavage was proposed in line with experimental data and DFT calculations.
A new catalyst for the asymmetric Henry reaction: Synthesis of β-nitroethanols in high enantiomeric excess
White, James D.,Shaw, Subrata
, p. 6270 - 6273 (2013/02/23)
A new chiral tetrahydrosalen ligand has been designed and synthesized from cis-2,5-diaminobicyclo[2.2.2]octane. The complex generated in situ by the interaction of the ligand with (CuOTf)2·C6H 5CH3 was an efficient catalyst for the asymmetric Henry reaction, producing nitroaldol products in high yield and good stereoselectivity. Henry reactions catalyzed by this tetrahydrosalen-Cu(I) complex led to syntheses of β-adrenergic blocking agents (S)-toliprolol, (S)-moprolol, and (S)-propanolol.
