136834-21-4 Usage
Description
Adenosine, N-benzoyl-5'-O-[bis(4-Methoxyphenyl)phenylMethyl]-2'-deoxy-2'-fluorois a complex organic compound with a unique molecular structure. It is a nucleoside building block derived from adenosine, a fundamental component of DNA and RNA. Adenosine, N-benzoyl-5'-O-[bis(4-Methoxyphenyl)phenylMethyl]-2'-deoxy-2'-fluorohas been modified with a benzoyl group, a bis(4-methoxyphenyl)phenylmethyl group, and a fluorine atom at the 2' position, which distinguishes it from the natural adenosine molecule. These modifications may enhance its properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
Adenosine, N-benzoyl-5'-O-[bis(4-Methoxyphenyl)phenylMethyl]-2'-deoxy-2'-fluorois used as a nucleoside building block for the preparation of 3'',4''-oxetane nucleosides. The application reason is its potential anti-viral properties, particularly towards Hepatitis C. The unique molecular structure of this compound may provide a new approach to developing effective treatments for this viral infection.
In addition to its use in the pharmaceutical industry, this compound may also have potential applications in other fields, such as:
1. Chemical Research:
As a complex organic molecule, Adenosine, N-benzoyl-5'-O-[bis(4-Methoxyphenyl)phenylMethyl]-2'-deoxy-2'-fluorocould be used in chemical research to study the effects of its unique structure on various chemical reactions and interactions with other molecules.
2. Material Science:
The unique properties of this compound, such as its modified adenosine structure and the presence of fluorine, may make it a candidate for the development of new materials with specific characteristics, such as improved stability or reactivity.
3. Diagnostics:
The modified adenosine structure could potentially be utilized in the development of diagnostic tools or tests, particularly in the field of molecular biology, where the detection and analysis of specific nucleosides and nucleotides are crucial.
Check Digit Verification of cas no
The CAS Registry Mumber 136834-21-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,3 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136834-21:
(8*1)+(7*3)+(6*6)+(5*8)+(4*3)+(3*4)+(2*2)+(1*1)=134
134 % 10 = 4
So 136834-21-4 is a valid CAS Registry Number.
136834-21-4Relevant articles and documents
SALTS OF COMPOUNDS AND CRYSTALS THEREOF
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Paragraph 0054, (2020/03/05)
The present invention provides crystals of (1R,3R,15E,28R,29R,30R,31R,34R,36R,39S,41R)-29,41-Difluoro-34,39-bis(sulfanyl)-2,33,35,38,40,42-hexaoxa-4,6,9,11,13,18,20,22,25,27-decaaza-34λ5,39λ5-diphosphaoctacyclo[28.6.4.13,36/sup
CYCLIC DI-NUCLEOTIDES AS STIMULATOR OF INTERFERON GENES MODULATORS
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Paragraph 00832; 00833; 00834, (2019/03/17)
The present disclosure relates to a compound of formulae (I) or (II), or a pharmaceutically acceptable salt, a solvate, a hydrate thereof, a pharmaceutical composition comprising a compound of formulae (I) or (II), and use thereof, wherein various Markush
CYCLIC DI-NUCLEOTIDES COMPOUNDS FOR THE TREATMENT OF CANCER
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Page/Page column 61; 62, (2018/09/12)
Provided herein are compounds useful for the treatment of cancer.