22537-07-1 | 4-Penten-1-amine

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$122.00	$86.00
1g	95%	in stock	$203.00	$142.00
5g	95%	in stock	$667.00	$467.00
10g	95%	in stock	$1,132.00	$793.00
25g	95%	in stock	$2,004.00	$1,403.00

Description

• Catalog Number: AF32265
• Chemical Name: 4-Penten-1-amine
• CAS Number: 22537-07-1
• Molecular Formula: C5H11N
• Molecular Weight: 85.1475
• MDL Number: MFCD08437625
• SMILES: NCCCC=C

Computed Properties

• Complexity: 32.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 0.7

Upstream Synthesis Route

The versatile compound 4-Penten-1-amine plays a crucial role in chemical synthesis as a valuable building block for various organic reactions. Known for its double bond and amino group, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure enables it to participate in diverse transformations, including nucleophilic addition, cross-coupling reactions, and ring-closing reactions. Additionally, 4-Penten-1-amine can be utilized for the synthesis of functionalized molecules with tailored properties, making it an indispensable tool in modern organic chemistry.

Literature

• Formation of Pent-4-en-1-amine, the counterpart of acrylamide from lysine and its conversion into piperidine in lysine/glucose reaction mixtures.

  Journal of agricultural and food chemistry 20100414

• Plasmodium falciparum spermidine synthase inhibition results in unique perturbation-specific effects observed on transcript, protein and metabolite levels.

  BMC genomics 20100101

• 5-Exo versus 6-endo cyclization of primary aminyl radicals: an experimental and theoretical investigation.

  The Journal of organic chemistry 20071221

• 3,3'-Bis(trisarylsilyl)-substituted binaphtholate rare earth metal catalysts for asymmetric hydroamination.

  Journal of the American Chemical Society 20060322

• Control of spermidine and spermine levels in rat tissues by trans-4-methylcyclohexylamine, a spermidine-synthase inhibitor.

  Biological & pharmaceutical bulletin 20050401

• Mammalian spermidine synthase--identification of cysteine residues and investigation of the putrescine binding site--.

  Biological & pharmaceutical bulletin 20040901