891491-99-9 Usage
Description
(6-(Dimethylamino)naphthalen-2-yl)methanol is a chemical compound with the molecular formula C14H15NO. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and contains a dimethylamino group and a hydroxymethyl group. (6-(DiMethylaMino)naphthalen-2-yl)Methanol is often used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active molecules.
Uses
Used in Organic Synthesis:
(6-(Dimethylamino)naphthalen-2-yl)methanol is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the development of new compounds with potential applications in various fields.
Used in Pharmaceutical Research:
In pharmaceutical research, (6-(Dimethylamino)naphthalen-2-yl)methanol is used as a key component in the synthesis of drugs. Its presence in the molecular structure can contribute to the desired pharmacological properties of the final product.
Used in Fluorescent Dyes Production:
(6-(Dimethylamino)naphthalen-2-yl)methanol is used as a reagent in the production of fluorescent dyes. Its chemical properties make it suitable for creating dyes that can be used in various applications, such as bioimaging and diagnostics.
Used in Optical Brighteners Production:
(6-(DiMethylaMino)naphthalen-2-yl)Methanol is also used in the production of optical brighteners, which are additives used to make materials appear brighter and more vivid. Its role in the synthesis process contributes to the development of effective brightening agents.
Used in Material Development:
(6-(Dimethylamino)naphthalen-2-yl)methanol has potential applications in the development of new materials. Its unique chemical structure can be utilized to create innovative materials with specific properties for various industries.
Used as a Chemical Probe in Biological Studies:
In biological studies, (6-(Dimethylamino)naphthalen-2-yl)methanol can be used as a chemical probe to investigate biological processes and interactions. Its ability to bind with certain molecules can provide valuable insights into the mechanisms of various biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 891491-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,1,4,9 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 891491-99:
(8*8)+(7*9)+(6*1)+(5*4)+(4*9)+(3*1)+(2*9)+(1*9)=219
219 % 10 = 9
So 891491-99-9 is a valid CAS Registry Number.
891491-99-9Relevant articles and documents
Histone deacetylase fluorescence probe, and preparation method and applications thereof
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, (2018/07/30)
The invention provides a histone deacetylase fluorescence probe, and a preparation method and applications thereof. The structure formula of the histone deacetylase fluorescence probe is disclosed inthe invention. In synthesis, 6-(dimethylamino)-2-naphthaldehyde with two-photon effect is selected as a dye, so that further nucleophilic reaction is realized after deacetylation reaction, and fluorescence signals are generated; aldehyde group carbon is modified into cyanogroup alcohol structures, hydroxyl is connected with HDACs responsive groups, and the histone deacetylase fluorescence probe isused for detecting and imaging of the activity of histone deacetylase in tissue. According to the histone deacetylase fluorescence probe, cyanogroup with excellent electron-withdrawing capability isintroduced, so that after response of HDACs with the histone deacetylase fluorescence probe, intramolecular cyclization reaction is carried out rapidly, activation of fluorescence signals is realized,detecting and imaging on histone deacetylase in living cells and tissue are realized, and excellent clinical application value is achieved.
Prodan-containing nucleotide and use thereof
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Page/Page column 18; sheet 2, (2008/06/13)
A compound represented by formula (1): wherein R1 is a substituent represented by formula (2): wherein R2 is ═O or —NH2, with the proviso that when R2 is ═O, H is attached to the 1-position N of the pyrimidine ring, and the bond between the 1-position N and the 6-position C is a single bond; or a substituent represented by formula (3): wherein R3 is —OH, ═O, or —NH2, with the proviso that when R3 is —OH or —NH2, R4 is H; when R3 is ═O, R4 is —NH2; and when R3 is ═O, H is attached to the 1-position N of the purine ring, and the bond between the 1-position N and the 6-position C is a single bond.
