6361-21-3 Usage
Description
2-Chloro-5-nitrobenzaldehyde is an organic compound characterized by its light yellow to beige-yellow crystalline powder appearance. It is known for its ability to undergo various chemical reactions, such as condensation with 2-methyl-1-propenylbenzimidazole to yield (E,Z)-2-(2-chloro-5-nitrostyryl)-1-(1-propenyl)benzimidazole and reacting with 5-aminopyrazoles to produce symmetrical bispyrazolo[3,4-]pyridines.
Uses
Used in Chemical Synthesis:
2-Chloro-5-nitrobenzaldehyde is used as a key intermediate in the synthesis of various organic compounds, including 5-nitro-2-(1H-pyrrol-1-yl)benzaldehyde. Its reactivity and structural properties make it a valuable building block for creating complex molecules in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloro-5-nitrobenzaldehyde is utilized as a starting material for the development of new drugs and medicinal compounds. Its versatile chemical properties allow for the creation of a wide range of therapeutic agents, potentially contributing to the treatment of various diseases and medical conditions.
Used in Dye and Pigment Industry:
2-Chloro-5-nitrobenzaldehyde can also be employed in the dye and pigment industry, where its unique chemical structure and properties can be harnessed to produce a variety of colorants and pigments for various applications, such as textiles, plastics, and printing inks.
Used in Research and Development:
In the field of research and development, 2-Chloro-5-nitrobenzaldehyde serves as an important compound for studying various chemical reactions and mechanisms. Its use in academic and industrial research can lead to the discovery of new synthetic methods, applications, and insights into the behavior of related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 6361-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6361-21:
(6*6)+(5*3)+(4*6)+(3*1)+(2*2)+(1*1)=83
83 % 10 = 3
So 6361-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClNO3/c8-7-2-1-6(9(11)12)3-5(7)4-10/h1-4H
6361-21-3Relevant articles and documents
NEW FYN AND VEGFR2 KINASE INHIBITORS
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Page/Page column 25; 26, (2021/06/22)
The invention relates to a N-phenylcarbamoyl compound of Formula (I) or a pharmaceutically acceptable salt thereof for use in the inhibition of at least one of tyrosine kinase selected from Fyn and VEGFR2 in the treatment of diseases and disorders involved with one or both kinases. (Formula)
Efficient and Highly Selective Solvent-Free Oxidation of Primary Alcohols to Aldehydes Using Bucky Nanodiamond
Lin, Yangming,Wu, Kuang-Hsu Tim,Yu, Linhui,Heumann, Saskia,Su, Dang Sheng
, p. 3497 - 3505 (2017/09/15)
Selective oxidation of alcohols to aldehydes is widely applicable to the synthesis of various green chemicals. The poor chemoselectivity for complicated primary aldehydes over state-of-the-art metal-free or metal-based catalysts represents a major obstacle for industrial application. Bucky nanodiamond is a potential green catalyst that exhibits excellent chemoselectivity and cycling stability for the selective oxidation of primary alcohols in diverse structures (22 examples, including aromatic, substituted aromatic, unsaturated, heterocyclic, and linear chain alcohols) to their corresponding aldehydes. The results are comparable to reported transition-metal catalysts including conventional Pt/C and Ru/C catalysts for certain substrates under solvent-free conditions. The possible activation process of the oxidant and substrates by the surface oxygen groups and defect species are revealed with model catalysts, ex situ electrochemical measurements, and ex situ attenuated total reflectance. The zigzag edges of sp2 carbon planes are shown to play a key role in these reactions.
Isoquinoline compound melanocortin receptor ligands and methods of using same
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, (2008/06/13)
The invention relates to melanocortin receptor ligands and methods of using the ligands to alter or regulate the activity of a melanocortin receptor. The invention further relates to tetrahydroisoquinoline aromatic amines that function as melanocortin receptor ligands and as agents for controlling cytokine-regulated physiologic processes and pathologies, and combinatorial libraries thereof.
