1020575-89-6 Usage
Description
1-(5-Bromo-2-nitro-phenyl)-ethanol is a chemical compound characterized by its molecular formula C8H8BrNO3. It presents as a white to light yellow crystalline powder and is recognized for its utility in the synthesis of pharmaceuticals and organic compounds. 1-(5-Bromo-2-nitro-phenyl)-ethanol is particularly notable for its role as a chiral building block, which is instrumental in the production of chiral ligands, catalysts, and potential drug candidates. Its structural properties also endow it with antimicrobial and antifungal capabilities, further expanding its applications across various sectors.
Uses
Used in Pharmaceutical Synthesis:
1-(5-Bromo-2-nitro-phenyl)-ethanol is used as a chiral building block for the synthesis of pharmaceuticals. Its unique structure allows for the creation of chiral ligands, catalysts, and potential drug candidates, making it a valuable component in the development of new medications.
Used in Organic Compound Synthesis:
In the field of organic chemistry, 1-(5-Bromo-2-nitro-phenyl)-ethanol serves as a key component in the synthesis of various organic compounds. Its versatility in chemical reactions contributes to the development of a wide range of products.
Used in Medicine and Biotechnology:
1-(5-Bromo-2-nitro-phenyl)-ethanol is used as an antimicrobial and antifungal agent in the medical and biotechnology industries. Its ability to combat microorganisms and fungi makes it a potentially useful substance in the development of treatments for various infections and diseases.
Used in Research and Development:
This chemical compound is also utilized as a reagent in the preparation of bioactive molecules and pharmaceutical intermediates. Its involvement in research and development underscores its importance in advancing scientific knowledge and innovation within the pharmaceutical and biotechnology sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 1020575-89-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,5,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1020575-89:
(9*1)+(8*0)+(7*2)+(6*0)+(5*5)+(4*7)+(3*5)+(2*8)+(1*9)=116
116 % 10 = 6
So 1020575-89-6 is a valid CAS Registry Number.
1020575-89-6Relevant articles and documents
Design and synthesis of a new chromophore, 2-(4-nitrophenyl)benzofuran, for two-photon uncaging using near-IR light
Komori, Naomitsu,Jakkampudi, Satish,Motoishi, Ryusei,Abe, Manabu,Kamada, Kenji,Furukawa, Ko,Katan, Claudine,Sawada, Wakako,Takahashi, Noriko,Kasai, Haruo,Xue, Bing,Kobayashi, Takayoshi
, p. 331 - 334 (2016)
A new chromophore, 2-(4-nitrophenyl)benzofuran (NPBF), was designed for two-photon (TP) uncaging using near-IR light. The TP absorption (TPA) cross-sections of the newly designed NPBF chromophore were determined to be 18 GM at 720 nm and 54 GM at 740 nm in DMSO. The TP uncaging reaction of a caged benzoate with the NPBF chromophore quantitatively produced benzoic acid with an efficiency (δu) of ～5.0 GM at 740 nm. The TP fragmentation of an EGTA unit was observed with δu = 16 GM. This behavior makes the new chromophore a promising TP photoremovable protecting group for physiological studies.
FUSED QUADRACYCLIC COMPOUNDS, COMPOSITIONS AND USES THEREOF
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Paragraph 0673, (2017/08/01)
Provided herein are substituted fused quadracyclic compounds useful as inhibitors of MK2. The invention further provides pharmaceutical compositions of the compounds of the invention. The invention also provides medical uses of substituted fused quadracyclic compounds.
Photolabile compound and substrate for oligomer probe array with the same
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Page/Page column 13, (2009/08/14)
Provided is a substrate for an oligomer probe array to which a photolabile material having an acetylene derivative is directly attached or attached via a linker.
