Name: Name:Piperonylamine
Brand: AABLOCKS
SKU: AA002S6Q
Rating: 90 (10 reviews)

Catalog No.: AA002S6Q

2620-50-0 | Piperonylamine

Pack Size： 1g

Purity： 90%

in stock

$18.00 $13.00

Pack Size： 5g

Purity： 95%

in stock

$25.00 $18.00

Pack Size： 10g

Purity： 95%

in stock

$31.00 $22.00

Pack Size： 25g

Purity： 95%

in stock

$75.00 $53.00

Pack Size： 100g

Purity： 95%

in stock

$293.00 $205.00

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Technical Information

Catalog Number: AA002S6Q

Chemical Name: Piperonylamine

CAS Number: 2620-50-0

Molecular Formula: C8H9NO2

Molecular Weight: 151.1626

MDL Number: MFCD00005840

SMILES: NCc1ccc2c(c1)OCO2

NSC Number: 75851

Properties

BP: 267°C at 760 mmHg

Form: Liquid

Refractive Index: n20/D 1.564(lit.)

Stability: Air Sensitive

Storage: Inert atmosphere;2-8℃;

Complexity: 140

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 11

Hydrogen Bond Acceptor Count: 3

Hydrogen Bond Donor Count: 1

Isotope Atom Count: 0

Rotatable Bond Count: 1

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 0.8

Literature fold

Title: Synthesis and anti-mycobacterial activity of novel amino alcohol derivatives.

Journal: European journal of medicinal chemistry20110301

Title: Characterization of the East Asian variant of aldehyde dehydrogenase-2: bioactivation of nitroglycerin and effects of Alda-1.

Journal: The Journal of biological chemistry20100108

Title: Design and Synthesis of Imidazopyrimidine Derivatives as Potent iNOS Dimerization Inhibitors.

Journal: The open medicinal chemistry journal20090101

Title: Resistance-modifying agents. 11.(1) Pyrimido[5,4-d]pyrimidine modulators of antitumor drug activity. Synthesis and structure-activity relationships for nucleoside transport inhibition and binding to alpha1-acid glycoprotein.

Journal: Journal of medicinal chemistry20040923

Title: New designer drug 1-(3,4-methylenedioxybenzyl) piperazine (MDBP): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry.

Journal: Journal of mass spectrometry : JMS20040301