Catalog No.:AA003EJM

73930-39-9 | 1-Phenylcyclopropanamine, HCl

Name: Name:1-Phenylcyclopropanamine, HCl
Brand: AABLOCKS
SKU: AA003EJM
Availability: InStock
Rating: 90 (10 reviews)

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250mg

97%

in stock

$21.00 $15.00

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97%

in stock

$37.00 $26.00

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97%

in stock

$141.00 $99.00

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003EJM

Chemical Name:

1-Phenylcyclopropanamine, HCl

CAS Number:

73930-39-9

Molecular Formula:

C9H12ClN

Molecular Weight:

169.6513

MDL Number:

MFCD07995722

SMILES:

NC1(CC1)c1ccccc1.Cl

Properties

BP:

211.4 °C at 760 mmHg

Form:

Solid

MP:

194.7 - 194.9 °C

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

121

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

Upstream Synthesis Route

6120-95-2

73930-39-9

[1]Patent:WO2006/86773,2006,A2,.Locationinpatent:Page/Pagecolumn32-34

[2]Patent:WO2011/119704,2011,A1,.Locationinpatent:Page/Pagecolumn35-36

[3]SyntheticCommunications,1980,vol.10,#2,p.107-110

925-90-6

100-47-0

73930-39-9

[1]Patent:US2015/105358,2015,A1,.Locationinpatent:Paragraph0411

[2]Patent:US2015/150871,2015,A1,.Locationinpatent:Paragraph0269

[3]Patent:WO2016/7423,2016,A1,.Locationinpatent:Page/Pagecolumn41;42

[4]Patent:WO2016/90230,2016,A1,.Locationinpatent:Page/Pagecolumn19-20

[5]Patent:US2017/114023,2017,A1,.Locationinpatent:Paragraph0117;0118

[6]Patent:WO2017/143237,2017,A1,.Locationinpatent:Page/Pagecolumn53;54

[7]Patent:WO2017/214565,2017,A1,.Locationinpatent:Page/Pagecolumn38

100-47-0

73930-39-9

[1]Patent:US2015/99744,2015,A1,

[2]Patent:US2015/105409,2015,A1,

[3]Patent:US2015/105383,2015,A1,

[4]Patent:WO2016/87950,2016,A1,.Locationinpatent:Page/Pagecolumn30

41049-53-0

73930-39-9

[1]Patent:US2015/99744,2015,A1,.Locationinpatent:Paragraph0251

[2]Patent:US2015/105409,2015,A1,.Locationinpatent:Paragraph0217-0219

[3]Patent:US2015/105383,2015,A1,.Locationinpatent:Paragraph0230-0231

75-16-1

100-47-0

73930-39-9

[1]Patent:WO2017/184774,2017,A1,.Locationinpatent:Page/Pagecolumn48

Downstream Synthesis Route

63201-02-5

73930-39-9

[1]SyntheticCommunications,1980,vol.10,p.107-110

73930-39-9

279215-55-3

(2-chloro-7,7-dioxo-4,7-dihydro-1,7λ6-dithia-4,6-diaza-inden-5-yl)-(1-phenyl-cyclopropyl)-amine

[1]JournalofMedicinalChemistry,2006,vol.49,p.4127-4139

6120-95-2

73930-39-9

[1]Patent:WO2006/86773,2006,A2.Locationinpatent:Page/Pagecolumn32-34

[2]Patent:WO2011/119704,2011,A1.Locationinpatent:Page/Pagecolumn35-36

[3]SyntheticCommunications,1980,vol.10,p.107-110

[4]ChemMedChem,2020,vol.15,p.643-658

773-64-8

73930-39-9

905912-11-0

[1]Patent:WO2006/86773,2006,A2.Locationinpatent:Page/Pagecolumn32-34

1215106-60-7

73930-39-9

1215105-18-2

[1]Patent:WO2010/30538,2010,A2.Locationinpatent:Page/Pagecolumn129-130

Literature

Title: Inactivation of C30A trimethylamine dehydrogenase by N-cyclopropyl-alpha-methylbenzylamine, 1-phenylcyclopropylamine, and phenylhydrazine.

Journal: Biochemistry 20010724

Title: Inactivation of monoamine oxidase B by 1-phenylcyclopropylamine: mass spectral evidence for the flavin adduct.

Journal: Bioorganic & medicinal chemistry letters 20010709

Title: Spectrometric evidence for the flavin-1-phenylcyclopropylamine inactivator adduct with monoamine oxidase N.

Journal: Biochemistry 20010508

Title: Determination of the role of serotonergic and cholinergic systems in apomorphine--induced aggressiveness in rats.

Journal: Polish journal of pharmacology and pharmacy 19790101

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