62347-97-1 Usage
Uses
Used in Organic Synthesis:
[4-(Methylamino)-3-nitrophenyl]methanol is used as a building block in the synthesis of various organic compounds. Its unique functional groups allow for versatile chemical reactions, making it a valuable intermediate in the production of specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [4-(Methylamino)-3-nitrophenyl]methanol is used as a key intermediate in the development of new drugs. Its structural features can be incorporated into medicinal compounds to modulate their biological activity and improve therapeutic efficacy.
Used in Dye and Pigment Manufacturing:
[4-(Methylamino)-3-nitrophenyl]methanol also has potential applications in the manufacturing of dyes and pigments. Its chemical structure can contribute to the color properties and stability of these products, offering new possibilities for colorants in various industries.
Safety Precautions:
It is crucial to handle [4-(Methylamino)-3-nitrophenyl]methanol with care and follow safety protocols to minimize health hazards. Proper protective equipment and handling procedures should be employed to ensure the safe use of [4-(Methylamino)-3-nitrophenyl]methanol in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62347-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,4 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62347-97:
(7*6)+(6*2)+(5*3)+(4*4)+(3*7)+(2*9)+(1*7)=131
131 % 10 = 1
So 62347-97-1 is a valid CAS Registry Number.
62347-97-1Relevant academic research and scientific papers
BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS
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Page/Page column 70, (2016/10/24)
Compounds of formula (I) and salts thereof: wherein R1, R2, R3, R4 are defined herein. Compounds of formula (I) and salts thereof have been found to inhibit the binding of the BET family of bromodomain proteins to, for example, acetylated lysine residues and thus may have use in therapy, for example in the treatment of autoimmune and inflammatory diseases, such as rheumatoid arthritis; and cancers.
Artificial redox enzymes
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, (2008/06/13)
Artificial redox enzymes are disclosed wherein one or more redox coenzymes or cofactors are linked to the 2-O, 3-O or 6-O positions of a D-glucopyranose ring of α-, β-, or γ-cyclodextrins. Also disclosed are facile synthetic methods for producing said art
Artificial Redox Enzymes. 1. Synthetic Strategies
Rong, Ding,Ye, Hongping,Boehlow, Todd R.,D'Souza, Valerian T.
, p. 163 - 167 (2007/10/02)
Organic models of flavoenzymes consist of a binding site covalently attached to a flavin derivative acting as the catalytic site.The earlier reported synthesis of such a model using α-cyclodextrin as the binding site proved to be difficult to reproduce wi
