19255-48-2 Usage
Description
9-(2-Chloro-ethyl)-9H-purin-6-ylamine, with the CAS number 19255-48-2, is an off-white solid compound that is utilized in various organic synthesis processes. It is a derivative of purine, an important component in the structure of nucleic acids and ATP, and features a chloro-ethyl group attached to the 9th position of the purine ring.
Uses
Used in Pharmaceutical Industry:
9-(2-Chloro-ethyl)-9H-purin-6-ylamine is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique chemical structure allows it to be a versatile building block in the development of new drugs targeting different therapeutic areas.
Used in Chemical Research:
In the field of chemical research, 9-(2-Chloro-ethyl)-9H-purin-6-ylamine is used as a research compound for [application reason]. It aids scientists in understanding the interactions and reactions of purine derivatives, which can lead to the discovery of novel chemical reactions and applications.
Used in Organic Synthesis:
9-(2-Chloro-ethyl)-9H-purin-6-ylamine is used as a key component in organic synthesis for [application reason]. Its chloro-ethyl group provides a reactive handle for further functionalization, making it a valuable precursor in the creation of complex organic molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19255-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,5 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19255-48:
(7*1)+(6*9)+(5*2)+(4*5)+(3*5)+(2*4)+(1*8)=122
122 % 10 = 2
So 19255-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8ClN5/c8-1-2-13-4-12-5-6(9)10-3-11-7(5)13/h3-4H,1-2H2,(H2,9,10,11)
19255-48-2Relevant articles and documents
Synthesis of adenine derivatives containing an amino alcohol fragment
Alksnis,Lidak
, p. 333 - 337 (1996)
The alkylation of adenine and N(6)-substituted adenine derivatives by 1,2-dihaloethanes and the production of 9-(2-haloethyl)derivatives of adenine were studied. In the reaction of the derivatives with amino alcohols a series of adenine derivat
Synthesis, cyclopolymerization and cyclo-copolymerization of 9-(2-Diallylaminoethyl)adenine and Its Hydrochloride Salt
Bouhadir, Kamal H.,Abramian, Lara,Ezzeddine, Alaa,Usher, Karyn,Vladimirov, Nikolay
, p. 13290 - 13306 (2012)
We report herein the synthesis and characterization of 9-(2- diallylaminoethyl) adenine. We evaluated two different synthetic routes starting with adenine where the optimal route was achieved through coupling of 9-(2-chloroethyl)adenine with diallylamine.
-
Okubo et al.
, p. 321 (1973)
-
Crystal of 5-( (2-(6-amino)-9H-purin-9-yl) ethyl) amino) pentan-1-o1
-
Paragraph 0061; 0062; 0063, (2018/02/28)
The present invention provides a new crystal form of 5-((2-(6-amino)-9H-purin-9-yl)ethyl)amino)pentan-1-ol, which has a relatively better effect in selectively inhibiting adenylate cyclase 1 and is capable of preparing a medicament for treating neuropathi
Two simple protocols for the preparation of diallylaminoethyl-substituted nucleic bases: A comparison
Shatila, Rania S.,Bouhadir, Kamal H.
, p. 1767 - 1770 (2007/10/03)
The syntheses of pyrimidine and purine nucleic bases substituted with diallylaminoethyl groups are reported following two different protocols. A comparison is made between the yield, expense, and difficulty of each route.
