26728-58-5

Basic information

• Product Name: 3-METHYL-2-BUTENE-1-AMINE HCL
• Synonyms: DIMETHYLALLYLAMINE HCL;3-METHYL-2-BUTENE-1-AMINE HCL;3-Methyl-2-butene-1-amine hydrochloride;N,N-Dimethylallylamine hydrochloride;2-ISOPENTENYLAMINE HYDROCHLORIDE (iPA.HCl);3-Methyl-2-buten-1-amine hydrochloride
• CAS NO: 26728-58-5
• Molecular Formula: C₅H₁₁N*ClH
• Molecular Weight: 121.61
• Mol File: 26728-58-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 193-194 °C (decomp)
• Boiling Point: 114.1 °C at 760 mmHg
• Flash Point: 19.6 °C
• Appearance: /
• Density: 0.787 g/cm³
• CAS DataBase Reference: 3-METHYL-2-BUTENE-1-AMINE HCL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHYL-2-BUTENE-1-AMINE HCL(26728-58-5)
• EPA Substance Registry System: 3-METHYL-2-BUTENE-1-AMINE HCL(26728-58-5)

Safety Data

• Hazardous Substances Data: 26728-58-5(Hazardous Substances Data)

Usage

Uses

2-Isopentenylamine Hydrochloride is used in the preparation of N9-substituted N6-[(3-methylbut-2-en-1-yl)amino]purine derivatives for their biological activity in various cytokinin bioasays.

Upstream product

• 870-63-3 prenyl bromide 
• 556-82-1 3-methyl-2-buten-1-ol 
• 1191-16-8 3-methylbut-2-enyl acetate 
• 15936-45-5 N-prenylphthalimide 

Downstream Products

• 543-83-9 galegine 
• 20859-00-1 6-(3-Methyl-2-butenylamino)-2-methylthio-9-β-D-ribofuranosylpurin 
• 7724-76-7 6-N-(2-isopentenyl)adenosine 
• 2365-40-4 N₆-(2-isopentenyl)adenine 
• 53274-45-6 2-Methylthio-trans-ribosylzeatin 
• 6025-53-2 trans-zeatin 9-β-D-ribofuranoside 
• 1005348-16-2 N-(3,3-dimethylallyl)-N'-N-bis-Cbz-guanidine 
• 55289-73-1 N-(3-methylbut-2-en-1-yl)-4-nitrobenzamide 
• 1365566-19-3 C₁₈H₂₄NO₅P 
• 1365566-35-3 C₁₈H₂₄NO₃P 
• 1365566-49-9 C₁₈H₂₄NO₃P 
• 1262675-44-4 benzyl (5-iodo-4,4-dimethyltetrahydropyrimidin-2(1H)-ylidene)carbamate 
• 1262675-51-3 C₁₄H₁₉N₃O₂ 
• 146269-39-8 (E)-Caracasanamide 

Relevant articles and documents

Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides

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

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

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