193751-54-1

Basic information

• Product Name: N-1-Boc-amino-3-cyclopentene
• Synonyms: CYCLOPENT-3-ENYL-CARBAMIC ACID TERT-BUTYL ESTER;1-N-BOC-AMINO-3-CYCLOPENTENE;N-1-BOC-AMINO-3-CYCLOPENTENE;Carbamic acid, 3-cyclopenten-1-yl-, 1,1-dimethylethyl ester (9CI);tert-Butyl N-(1-cyclopent-3-enyl)carbamate;3-Cyclopenten-1-yl-carbaMic Acid 1,1-DiMethylethyl Ester;N-3-Cyclopenten-1-yl-carbaMic Acid 1,1-DiMethylethyl Ester;tert-Butyl 3-cyclopentenylcarbaMate
• CAS NO: 193751-54-1
• Molecular Formula: C₁₀H₁₇NO₂
• Molecular Weight: 183.25
• Product Categories: N-BOC;Amines;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 193751-54-1.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 268.877 °C at 760 mmHg
• Flash Point: 116.413 °C
• Appearance: /
• Density: 1.014 g/cm³
• Vapor Pressure: 0.00749mmHg at 25°C
• Refractive Index: 1.483
• Storage Temp.: 2-8°C
• PKA: 12.37±0.20(Predicted)
• CAS DataBase Reference: N-1-Boc-amino-3-cyclopentene(CAS DataBase Reference)
• NIST Chemistry Reference: N-1-Boc-amino-3-cyclopentene(193751-54-1)
• EPA Substance Registry System: N-1-Boc-amino-3-cyclopentene(193751-54-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 193751-54-1(Hazardous Substances Data)

Usage

Uses

N-1-Boc-amino-3-cyclopentene is a cyclopentenamine with a protecting group used to explore the feasibility of using small molecules to functionalize Si surfaces with primary amine groups for DNA attachment.

InChI:InChI=1/C10H17NO2/c1-10(2,3)13-9(12)11-8-6-4-5-7-8/h4-5,8H,6-7H2,1-3H3,(H,11,12)

Upstream product

• 71432-55-8 2-tert-butyl-1,3-diisopropylisourea 
• 219844-47-0 N-(t-butyloxycarbonyl)-N-(methanesulfonyloxy)cyclopent-3-enylcarboxamide 
• 75-65-0 tert-butyl alcohol 
• 2487-95-8 4-Isocyanato-cyclopentene 
• 91469-55-5 cyclopent-3-en-1-amine hydrogen chloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 14320-38-8 cyclopent-3-enol 
• 253680-54-5 methanesulfonic acid cyclopent-3-enyl ester 
• 1018908-86-5 (tert-butoxycarbonyl-cyclopent-3-enyl-amino)-oxo-acetic acid ethyl ester 
• 7686-77-3 3-cyclopentene-1-carboxylic acid 
• 216959-34-1 ethyl 2-{[(tert-butoxy)carbonyl]amino}-2-oxoacetate 

Downstream Products

• 1154870-59-3 (±)-trans-(3-hydroxycyclopentyl)carbamic acid tert-butyl ester 
• 1154870-59-3 (+/-)-cis-(3-hydroxy-cyclopentyl)-carbamic acid tert-butyl ester 
• 250659-32-6 racemic tert-butyl ((1R,3S,5S)-6-oxabicyclo[3.1.0]hexan-3-yl)carbamate 
• 216578-35-7 tert-butyl (1R,3R,5S)-6-oxabicyclo[3.1.0]hexan-3-ylcarbamate 
• 154802-92-3 (+/-)-1-hydroxy-4-[(tert-butoxycarbonyl)amino]-2-cyclopentene 
• 1154870-59-3 trans-(3-hydroxycyclopentyl)carbamic acid tert-butyl ester 
• 1154870-59-3 (cis-3-hydroxy-cyclopentyl)-carbamic acid tert-butyl ester 
• 1154870-59-3 (trans-3-hydroxy-cyclopentyl)-carbamic acid tert-butyl ester 
• 1552273-85-4 1-(cyclopent-3-en-1-yl)-5-(3-fluoro-4-(trifluoromethyl)phenyl)-1H-imidazole 
• 1552273-68-3 1-(cyclopent-3-en-1-yl)-5-phenyl-1H-imidazole 
• 1225384-36-0 benzyl (1S,3R,4S)-3,4-dihydroxycyclopentyl(methyl)carbamate 

Relevant articles and documents

POTENT AND HIGHLY SELECTIVE HETEROAROMATIC INHIBITORS OF NEURONAL NITRIC OXIDE SYNTHASE

Peptidomimetic compounds as can inhibit neuronal nitric oxide synthase (nNOS) for potential treatment in neurodegenerative diseases, such as but not limited to stroke, Alzheimer's disease, Parkinson's disease, Huntington's disease.

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Compounds inhibiting neuronal nitric oxide synthase (nNOS) for potential treatment in neurodegenerative diseases, such as stroke, Alzheimer's disease, Parkinson's disease, Huntington's disease, such compounds of a formula.

New route to 4-aminocyclopent-2-en-1-ols: Synthesis and enantioselective rearrangement of 4-amino-substituted cyclopentene oxides

A new route for the asymmetric synthesis of 4-aminocyclopent-2-en-1-ols (90% ee) for carbocyclic nucleoside analogue synthesis is described. The approach involves the stereoselective preparation of cis 4-amino-substituted cyclopentene oxides and subsequent chiral base-mediated rearrangement to the corresponding allylic alcohols. Full details on the synthesis and stereoselectivity of epoxidation of 4-amino-substituted cyclopentenes are presented. (C) 2000 Elsevier Science Ltd.