73289-91-5 Usage
Description
3-Ethyl-2-hydroxybenzaldehyde, also known as 3-Ethylsalicylaldehyde, is an organic compound with the molecular formula C9H10O2. It is a derivative of salicylaldehyde, featuring an ethyl group at the 3rd position and a hydroxyl group at the 2nd position. 3-ETHYL-2-HYDROXYBENZALDEHYDE is known for its distinct chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
3-Ethyl-2-hydroxybenzaldehyde is used as an intermediate in the synthesis of thiosemicarbazones, which are compounds with potential applications as inhibitors of lysophosphatidic acid acyltransferase (LPAAT). LPAAT inhibitors are of interest in the pharmaceutical industry due to their potential role in the treatment of various diseases, including cancer and metabolic disorders.
Additionally, 3-Ethyl-2-hydroxybenzaldehyde can be used in the development of new drugs and therapeutic agents, leveraging its unique chemical structure to target specific biological pathways and modulate cellular processes.
Used in Chemical Synthesis:
In the field of organic chemistry, 3-Ethyl-2-hydroxybenzaldehyde can be employed as a building block for the synthesis of various complex molecules and compounds. Its reactive functional groups, including the aldehyde and hydroxyl groups, allow for a range of chemical reactions, such as oxidation, reduction, and condensation, enabling the creation of diverse chemical products.
Used in Research and Development:
3-Ethyl-2-hydroxybenzaldehyde can also be utilized in research and development settings, where it can serve as a model compound for studying the properties and reactivity of similar organic molecules. This can contribute to the advancement of scientific knowledge and the development of new technologies and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 73289-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,8 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73289-91:
(7*7)+(6*3)+(5*2)+(4*8)+(3*9)+(2*9)+(1*1)=155
155 % 10 = 5
So 73289-91-5 is a valid CAS Registry Number.
73289-91-5Relevant articles and documents
CHEMICAL COMPOUNDS
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Paragraph 0286-0288, (2021/01/23)
The present disclosure describes novel compounds, or their pharmaceutically acceptable salts, pharmaceutical compositions containing them, and their medical uses. Compounds of the disclosure have activity as dual modulators of Janus kinase (JAK), alone, or in combination with one or more of an additional mechanism, including a tyrosine kinase, such as TrkA or Syk, and PDE4, and are useful in the in the treatment or control of inflammation, auto-immune diseases, cancer, and other disorders and indications where modulation of JAK would be desirable. Also described herein are methods of treating inflammation, auto-immune diseases, cancer, and other conditions susceptible to inhibition of JAK and PDE4 by administering a compound herein described.
Efficient synthesis of chiral benzofuryl β-amino alcohols via a catalytic asymmetric Henry reaction
Chen, Wei,Zhou, Zhao-Hui,Chen, Hong-Bin
supporting information, p. 1530 - 1536 (2017/02/15)
Chiral β-amino alcohol ligands were found effective for the copper(ii)-catalyzed asymmetric Henry reaction of benzofuran-2-carbaldehydes with nitromethane, which led to the formation of (S)-enriched benzofuryl β-nitro alcohols with satisfactory enantioselectivities (up to 98% ee). Using this catalytic protocol, bioactive (S)-benzofuryl β-amino alcohols could be conveniently prepared in short steps.
New chemo-enzymatic approaches for the synthesis of (R)- and (S)-bufuralol
Nagy, Botond,Dima, Norbert,Paizs, Csaba,Brem, Jürgen,Irimie, Florin Dan,Toa, Monica Ioana
, p. 1316 - 1322 (2015/01/09)
Both enantiomers of bufuralol are pharmaceutically important molecules. While the (S)-isomer with a higher β-blocking activity is recommended for hypertension treatment, the (R)-enantiomer can be used as marker of hepatic activity. In this paper two new a
