6443-72-7 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Dimethoxycinnamonitrile is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Synthesis:
In the field of organic chemistry, 3,4-Dimethoxycinnamonitrile serves as a versatile building block for the creation of a wide range of organic molecules. Its reactivity and functional groups make it suitable for use in the synthesis of complex organic compounds, including those with potential applications in materials science, agrochemicals, and specialty chemicals.
Used in Flavor and Fragrance Industry:
3,4-Dimethoxycinnamonitrile is used as a starting material for the production of various flavor and fragrance compounds. Its aromatic properties and ability to undergo chemical transformations make it a valuable component in the creation of unique scents and tastes for the food, beverage, and cosmetic industries.
Used in Research and Development:
3,4-Dimethoxycinnamonitrile is utilized in research laboratories for the study of chemical reactions and the development of new synthetic methods. Its unique properties and reactivity make it an interesting subject for scientific investigation, potentially leading to new discoveries and advancements in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6443-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,4 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6443-72:
(6*6)+(5*4)+(4*4)+(3*3)+(2*7)+(1*2)=97
97 % 10 = 7
So 6443-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)/p-1/b6-4+
6443-72-7Relevant academic research and scientific papers
Modular Approach to 9-Monosubstituted Fluorene Derivatives Using MoV Reagents
Franzmann, Peter,Trosien, Simon,Schubert, Moritz,Waldvogel, Siegfried R.
supporting information, p. 1182 - 1185 (2016/03/15)
Oxidative coupling using molybdenum(V) reagents provides fast access to highly functionalized 9-monosubstituted fluorenes. This synthetic approach is highly modular, is high yielding, and tolerates a variety of labile moieties, e.g. amides or iodo groups. The established protocol leads to promising precursors for pharmacologically important analogues of melatonin.
Pentaalkylstiboranes. 1. Synthesis of Homobenzylic Alcohols, Homoallylic Alcohols, Ethyl 5-Aryl-5-hydroxypent-2-enoates, and β-Hydroxypropionic Acid Derivatives via Pentaalkylstiboranes
Huang, Yao-Zeng,Liao, Yi
, p. 1381 - 1386 (2007/10/02)
Although pentaalkylstiboranes have long been known, their applications in organic synthesis have not been exploited.It has been found that quaternary stibonium salts (n-Bu3SbCH2E)+X- (E = Ph, CH=CH2, CH=CHCO2Et, CO2Et, CN; X = Br, I, BPh4) on treatment with RLi (R = n-Bu, t-Bu, Ph) afford pentaalkylstiboranes, n-Bu3Sb(R)CH2E, which react with aromatic aldehydes to give, after subsequent hydrolysis, homobenzylic alcohols, homoallylic alcohols, ethyl 5-aryl-5-hydroxypent-2-enoates, and β-aryl-β-hydroxypropionitriles, respectively, in good to excellent yields.The reaction is chemoselective for aldehydes.
