21473-21-2 Usage
Uses
Used in Nucleic Acid Research:
N(3)-benzylthymidine is used as a research tool for studying the structure and function of DNA and RNA. The benzyl group attached to the N(3) position of the thymine base may impart specific chemical and biological properties to the molecule, allowing for the investigation of nucleic acid interactions and mechanisms.
Used in Drug Development:
N(3)-benzylthymidine is used as a potential candidate for developing novel antiviral or anticancer drugs targeting nucleic acid metabolism. The synthetic nature of this compound allows for the exploration of its therapeutic potential in laboratory settings, with the aim of creating new treatments for various diseases.
Used in Laboratory Settings:
Due to its synthetic nature, N(3)-benzylthymidine is mainly used as a research tool in laboratory settings. This allows scientists to explore its properties and potential applications in a controlled environment, facilitating the advancement of nucleic acid research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 21473-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,7 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21473-21:
(7*2)+(6*1)+(5*4)+(4*7)+(3*3)+(2*2)+(1*1)=82
82 % 10 = 2
So 21473-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H20N2O5/c1-11-8-18(15-7-13(21)14(10-20)24-15)17(23)19(16(11)22)9-12-5-3-2-4-6-12/h2-6,8,13-15,20-21H,7,9-10H2,1H3/t13-,14+,15+/m0/s1
21473-21-2Relevant articles and documents
Preparation and pharmacological evaluation of N3-substituted thymidine derivatives as central depressants
Kimura,Watanabe,Tateoka,Kondo,Ing Kang Ho,Yamamoto
, p. 1180 - 1182 (1993)
Central depressant effects in mice of N3-substituted thymidines (Td) (1) were examined by intracerebroventricular (i.c.v.) injection. Nine derivatives including the methyl, ethyl, propyl, allyl, benzyl, xylyl and α-phenylethyl derivatives at th
Photoinduced Deoxygenative Borylations of Aliphatic Alcohols
Wu, Jingjing,B?r, Robin M.,Guo, Lin,Noble, Adam,Aggarwal, Varinder K.
supporting information, p. 18830 - 18834 (2019/11/22)
A photochemical method for converting aliphatic alcohols into boronic esters is described. Preactivation of the alcohol as a 2-iodophenyl-thionocarbonate enables a novel Barton–McCombie-type radical deoxygenation that proceeds efficiently with visible light irradiation and without the requirement for a photocatalyst, a radical initiator, or tin or silicon hydrides. The resultant alkyl radical is intercepted by bis(catecholato)diboron, furnishing boronic esters from a diverse range of structurally complex alcohols.
