34308-25-3 Usage
Uses
1-Methyladenosine Hydroiodide is used as a research chemical for [application reason]
Used in Pharmaceutical Research:
1-Methyladenosine Hydroiodide is used as a compound in the development of new pharmaceuticals, potentially for [specific therapeutic area or general purpose], due to its unique molecular structure and the possibility of interaction with biological systems.
Used in Chemical Synthesis:
1-Methyladenosine Hydroiodide is used as an intermediate in the synthesis of more complex molecules, which could be relevant in the fields of organic chemistry or materials science.
Used in Analytical Chemistry:
1-Methyladenosine Hydroiodide is used as a reference material or standard in analytical chemistry for the calibration of instruments or the development of new analytical methods.
Note: Since the provided materials do not specify the exact applications or industries where 1-Methyladenosine Hydroiodide is used, the above uses are hypothetical and based on the general properties of similar compounds. It is essential to consult material safety data sheets and applicable safety protocols when handling this or any chemical substance.
Check Digit Verification of cas no
The CAS Registry Mumber 34308-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34308-25:
(7*3)+(6*4)+(5*3)+(4*0)+(3*8)+(2*2)+(1*5)=93
93 % 10 = 3
So 34308-25-3 is a valid CAS Registry Number.
34308-25-3Relevant academic research and scientific papers
Aboul-Fadl, Tarek,Rajeev, Gopalan,Broom, Arthur D.
, p. 445 - 451 (2008)
(Chemical Equation Presented) A novel peptide nucleic acid (PNA) monomer 16 containing a novel 1-methyl-6-mercaptopurine base was synthesized by coupling the in situ generated acid chloride of (1-methyl-6-mercaptopurin-9-yl)acetic acid (6) into an L-lysine backbone (13) using 10% CCl4 in pyridine and Ph3P. Compound 6 was synthesized from 6-mercapto-1-methylpurine and ethylbromoacetate in the presence of NaH followed by alkaline hydrolysis and subsequent neutralization with a cation exchange resin. The L-lysine backbone (13) was obtained by the reaction of Nε-CBZ-L-lysine allyl ester with Boc-aminoactaldehyde in the presence of NaBH3CN under reductive amination conditions. Oligomerization of the monomer 16 to PNA analogues was achieved using BOC-BHA-PEG-PS resin as a solid support and the in situ generated acid chloride of 16 by 10% CCl4 in DCM in the presence of Ph 3P.
