128121-04-0

Basic information

• Product Name: (E)-4-aMino-2-Methylbut-2-en-1-olhydrochloride
• Synonyms: (E)-4-AMINO-2-METHYLBUT-2-EN-1-OL HYDROCHLORIDE
• CAS NO: 128121-04-0
• Molecular Formula: C5H12ClNO
• Molecular Weight: 137.60788
• Mol File: 128121-04-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-4-aMino-2-Methylbut-2-en-1-olhydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-aMino-2-Methylbut-2-en-1-olhydrochloride(128121-04-0)
• EPA Substance Registry System: (E)-4-aMino-2-Methylbut-2-en-1-olhydrochloride(128121-04-0)

Safety Data

• Hazardous Substances Data: 128121-04-0(Hazardous Substances Data)

Usage

General Description

(E)-4-Amino-2-methylbut-2-en-1-ol hydrochloride is a chemical compound with the molecular formula C5H11NO·HCl. It is a derivative of 2-methylbut-2-en-1-ol and is often used as a reagent in organic synthesis. (E)-4-aMino-2-Methylbut-2-en-1-olhydrochloride has been studied for its potential as a building block in the synthesis of pharmaceuticals and other biologically active compounds. It may also have applications in the development of new materials and in chemical research. (E)-4-Amino-2-methylbut-2-en-1-ol hydrochloride is a versatile and important compound in the field of organic chemistry.

Upstream product

• 128121-02-8 (trans)-4-[(t-butoxycarbonyl)amino]-2-methyl-2-butenoic acid 
• 356789-18-9 (E)-4-tert-butoxycarbonylamino-2-methylbut-2-enoic acid ethyl ester 
• 128121-03-9 (E)-tert-butyl (4-hydroxy-3-methylbut-2-en-1-yl)carbamate 

Relevant articles and documents

SYNTHESIS OF THE NATURALLY OCCURING CYTOKININ 2'-DEOXYZEATIN RIBOSIDE

2'-Deoxyzeatin riboside, previously isolated together with other three cytokinins from culture filtrates of the pathogenic bacterium Pseudomonas amygdali, has been synthesized by reaction of 6-chloro-9-(2-dexy-β-D-ribofuranosyl)purine with (E)-4-amino-2-methyl-but-2-en-1-ol.The identity of the synthetic and the naturally occuring cytokinin has been established.

Total synthesis of the alkaloids martinelline and martinellic acid via a hetero Diels-Alder multicomponent coupling reaction

(formula presented) A concise synthesis of the guanidine alkaloids, (±)-martinelline and (±)-martinellic acid, using a protic acid catalyzed 2:1 hetero Diels-Alder coupling reaction between N-Cbz 2-pyrroline and methyl 4-aminobenzoate, is described. Protic acid catalysis, rather than Lewis acid catalysis, was necessary to achieve the desired sense of diastereocontrol in the coupling reaction.