26728-58-5 Usage
Description
3-METHYL-2-BUTENE-1-AMINE HCL, also known as 2-Isopentenylamine Hydrochloride, is an organic compound with amine and hydrochloride functional groups. It is characterized by its unique chemical structure, which contributes to its specific properties and applications in various fields.
Uses
Used in Pharmaceutical Industry:
3-METHYL-2-BUTENE-1-AMINE HCL is used as a chemical intermediate for the synthesis of N9-substituted N6-[(3-methylbut-2-en-1-yl)amino]purine derivatives. These derivatives exhibit significant biological activity and are utilized in various cytokinin bioassays, which are essential for understanding the role of cytokinins in cell growth and development.
Used in Research and Development:
In the field of research and development, 3-METHYL-2-BUTENE-1-AMINE HCL serves as a key compound for the exploration of new drug candidates and the study of their interactions with biological systems. Its unique chemical structure allows for the development of novel therapeutic agents with potential applications in various medical conditions.
Used in Chemical Synthesis:
3-METHYL-2-BUTENE-1-AMINE HCL is also employed in the chemical synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its versatile reactivity and functional groups make it a valuable building block for the creation of complex molecular structures with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 26728-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,2 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26728-58:
(7*2)+(6*6)+(5*7)+(4*2)+(3*8)+(2*5)+(1*8)=135
135 % 10 = 5
So 26728-58-5 is a valid CAS Registry Number.
26728-58-5Relevant articles and documents
Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides
Soltanzadeh, Bardia,Jaganathan, Arvind,Staples, Richard J.,Borhan, Babak
supporting information, p. 9517 - 9522 (2015/08/11)
An organocatalytic and highly regio-, diastereo-, and enantioselective intermolecular haloetherification and haloesterification reaction of allyl amides is reported. A variety of alkene substituents and substitution patterns are compatible with this chemistry. Notably, electronically unbiased alkene substrates exhibit exquisite regio- and diastereoselectivity for the title transformation. We also demonstrate that the same catalytic system can be used in both chlorination and bromination reactions of allyl amides with a variety of nucleophiles with little or no modification. A highly regioselective intermolecular haloetherification that proceeds with excellent enantioselectivity, catalyzed by cinchona alkaloid dimers, is reported. The regioselectivity is preserved for unbiased alkyl substituted allyl amides with either E or Z geometry. (DHQD)2PHAL=hydroquinidine 1,4-phthalazinediyl diether.
WEIGHT REDUCING COMPOUNDS
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Page/Page column 15; 16, (2009/09/04)
The present invention relates to compounds which find use as weight reducing agents, and find use in treating obesity and/or excess adiposity.
Synthesis of Amido-ureas and the Nature of Caracasanamide, the Hypotensive Principle of Verbesina caracasana
Crombie, Leslie,Jarrett, Sandra R. M.
, p. 3179 - 3184 (2007/10/02)
Syntheses of the (E)-1 and (Z)-2 forms of 1-(3-methylbut-2-enyl)-3-(4-butyl)urea, proposed structures for the natural hypotensive caracasanamide, have been carried out.The compounds were found not to be identical wit