What is the 2-Amino-4-phenylbutane?

2-Amino-4-phenylbutane is colorless liquid, while it's Molecular Formula is C10H15N. colorless liquid 2-Amino-4-phenylbutane is used in the synthesis of N-substituted derivatives of (1-methyl-3- phenylpropyl)amine.

What is the CAS number for 2-Amino-4-phenylbutane?

The CAS number of 2-Amino-4-phenylbutane is 22374-89-6.

What is the 2-Amino-4-phenylbutane?

2-Amino-4-phenylbutane is colorless liquid, while it's Molecular Formula is C10H15N. colorless liquid 2-Amino-4-phenylbutane is used in the synthesis of N-substituted derivatives of (1-methyl-3- phenylpropyl)amine.

What is the CAS number for 2-Amino-4-phenylbutane?

The CAS number of 2-Amino-4-phenylbutane is 22374-89-6.

Product classification

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22374-89-6

Product Name:4-phenylbutan-2-amine
Molecular Formula:C₁₀H₁₅N
Molecular Weight:149.236
Appearance:colorless liquid

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Product Details

pd_meltingpoint:-50 °C

Appearance:colorless liquid

Purity:99%

Buy High Quality 4-phenylbutan-2-amine, Offer Good Quality 22374-89-6

Molecular Formula:C10H15N
Molecular Weight:149.236
Appearance/Colour:colorless liquid
Vapor Pressure:0.107mmHg at 25°C
Melting Point:-50 °C
Refractive Index:n20/D 1.514(lit.)
Boiling Point:221.5 °C at 760 mmHg
PKA:pKa 10.0 (Uncertain)
Flash Point:97.8 °C
PSA：26.02000
Density:0.936 g/cm³
LogP:2.66670

2-Amino-4-phenylbutane(Cas 22374-89-6) Usage

Chemical Properties	clear colorless liquid
Uses	2-Amino-4-phenylbutane is used in the synthesis of N-substituted derivatives of (1-methyl-3- phenylpropyl)amine.
Biological Functions	Amphetamine is an indirectly acting adrenomimetic amine that depends for its action on the release of norepinephrine from noradrenergic nerves. Its pharmacological effects are similar to those of ephedrine; however, its CNS stimulant activity is somewhat greater. Both systolic and diastolic blood pressures are increased by oral dosing with amphetamine. The heart rate is frequently slowed reflexively. Cardiac output may remain unchanged in the low- and moderate-dose range. The therapeutic uses of amphetamine are based on its ability to stimulate the CNS. The D-isomer (dextroamphetamine) is three to four times as potent as the L-isomer in producing CNS effects. It has been used in the treatment of obesity because of its anorexic effect, although tolerance to this effect develops rapidly. It prevents or overcomes fatigue and has been used as a CNS stimulant. Amphetamine is no longer recommended for these uses because of its potential for abuse. Amphetamine is useful in certain cases of narcolepsy or minimal brain dysfunction.
Flammability and Explosibility	Notclassified
Safety Profile	A poison by intraperitoneal and parenteral route. Moderately toxic by ingestion.When heated to decomposition it emits toxic vapors of NOx.
Consumer Uses	ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C10H15N/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6,9H,7-8,11H2,1H3/p+1/t9-/m0/s1

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22374-89-6 Process route

: 2550-26-7
4-Phenyl-2-butanone

: 100-46-9
benzylamine

: 22374-89-6,22148-77-2,1199266-89-1
(RS)-1-methyl-3-phenylpropylamine

: 100-52-7
benzaldehyde

Conditions

Conditions	Yield
With S-selective ω-transaminase from paracoccus denitrificans transaminase; NAD; aldehyde dehydrogenase; In dimethyl sulfoxide; Reagent/catalyst; Enzymatic reaction;