4-Penten-1-amine - CAS 22537-07-1

Catalog:	BB017660
Product Name:	4-Penten-1-amine
CAS:	22537-07-1
Synonyms:	Pent-4-enylamine

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BB017660	5 g	$398	In stock

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IUPAC Name:	pent-4-en-1-amine
Description:	In the presence of sugars, lysine, similarly to asparagine and phenylalanine, can undergo carbonyl-assisted decarboxylative deamination reaction to generate pent-4-en-1-amine, the counterpart of acrylamide.
Molecular Weight:	85.15
Molecular Formula:	C5H11N
Canonical SMILES:	C=CCCCN
InChI:	InChI=1S/C5H11N/c1-2-3-4-5-6/h2H,1,3-6H2
InChI Key:	UVBBCQLPTZEDHT-UHFFFAOYSA-N
Boiling Point:	96.1±9.0 °C at 760 mmHg
Density:	0.8±0.1 g/cm3
Appearance:	Colorless liquid
LogP:	1.61160

Publication Number	Title	Priority Date
CN-113209836-A	Composite separation membrane based on fluorine-containing copolymer in-situ growth organic frame structure and preparation method and application thereof	20210519
CN-113248971-A	Photosensitive electronic ink with high water resistance	20210424
CN-112441767-A	Preparation method of accelerator for spraying mortar/concrete	20201127
CN-112457234-A	Visible light promoted synthesis method of 2-selenomethylpyrrolidine compound	20201123
CN-111548526-A	Quaternary ammonium salt type dendritic polythioether modified polymer microsphere	20200625

PMID	Publication Date	Title	Journal
20205470	20100414	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
20385001	20100412	Plasmodium falciparum spermidine synthase inhibition results in unique perturbation-specific effects observed on transcript, protein and metabolite levels	BMC genomics
18001094	20071221	5-Exo versus 6-endo cyclization of primary aminyl radicals: an experimental and theoretical investigation	The Journal of organic chemistry
16536549	20060322	3,3'-Bis(trisarylsilyl)-substituted binaphtholate rare earth metal catalysts for asymmetric hydroamination	Journal of the American Chemical Society
15802788	20050401	Control of spermidine and spermine levels in rat tissues by trans-4-methylcyclohexylamine, a spermidine-synthase inhibitor	Biological & pharmaceutical bulletin

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GHS Hazard Statement:	H301 (95%): Toxic if swallowed [Danger Acute toxicity, oral]
Precautionary Statement:	P264, P270, P280, P301+P310, P305+P351+P338, P310, P321, P330, P405, and P501
Signal Word:	Danger

Complexity:	32.9
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	85.089149355
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	85.089149355
Rotatable Bond Count:	3
Topological Polar Surface Area:	26 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0.7