Catalog No.:AA003429

1126-09-6 | Ethyl piperidine-4-carboxylate

Name: Name:Ethyl piperidine-4-carboxylate
Brand: AABLOCKS
SKU: AA003429
Availability: InStock
Rating: 90 (10 reviews)

Pack Size

Purity

Availability

Price(USD)

Quantity

97%

in stock

$6.00 $4.00

- +

10g

97%

in stock

$7.00 $5.00

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25g

≥95%

in stock

$16.00 $11.00

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100g

95%

in stock

$23.00 $16.00

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500g

90%(GC)

in stock

$77.00 $54.00

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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:

AA003429

Chemical Name:

Ethyl piperidine-4-carboxylate

CAS Number:

1126-09-6

Molecular Formula:

C8H15NO2

Molecular Weight:

157.2102

MDL Number:

MFCD00006003

SMILES:

CCOC(=O)C1CCNCC1

NSC Number:

93792

Properties

BP:

204°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.459(lit.)

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

130

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.5

Upstream Synthesis Route

1126-09-6

6457-49-4

[1]Patent:WO2004/76450,2004,A1,.Locationinpatent:Page59

[2]Patent:WO2010/12611,2010,A1,.Locationinpatent:Page/Pagecolumn27

[3]RSCAdvances,2016,vol.6,#22,p.17929-17940

[4]EuropeanJournalofMedicinalChemistry,2019,p.234-248

[5]EuropeanJournalofMedicinalChemistry,2017,vol.139,p.773-791

[6]JournalofMedicinalChemistry,1991,vol.34,#3,p.1073-1079

[7]Patent:WO2008/119792,2008,A1,.Locationinpatent:Page/Pagecolumn68-69

[8]JournaloftheChemicalSociety,1937,p.1523,1525

[9]BioorganicandMedicinalChemistryLetters,1997,vol.7,#8,p.1047-1052

[10]JournalofLabelledCompoundsandRadiopharmaceuticals,1999,vol.42,#SUPPL.1,p.S782-S784

[11]Patent:US4925850,1990,A,

[12]Patent:US4931449,1990,A,

[13]Patent:US4977159,1990,A,

[14]Patent:US4885302,1989,A,

[15]Patent:US5821240,1998,A,

1570-45-2

6457-49-4

1126-09-6

[1]CollectionofCzechoslovakChemicalCommunications,1959,vol.24,p.212,216

1126-09-6

20691-89-8

[1]EuropeanJournalofOrganicChemistry,2006,#10,p.2314-2321

1126-09-6

22990-34-7

[1]BioorganicandMedicinalChemistryLetters,2012,vol.22,#22,p.6938-6942,5

1126-09-6

39546-32-2

[1]BioorganicandMedicinalChemistryLetters,2002,vol.12,#5,p.757-761

Downstream Synthesis Route

1126-09-6

64-17-5

7379-35-3

121912-29-6

[1]TetrahedronLetters,1984,vol.25,p.4521-4524

1126-09-6

452-62-0

1-(2-fluoro-5-methyl-phenyl)-piperidine-4-carboxylicacidethylester

[1]SyntheticCommunications,2003,vol.33,p.2145-2149

1126-09-6

62965-10-0

609367-77-3

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,p.2715-2718

1126-09-6

7379-35-3

121912-29-6

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4838-4841

[2]Patent:US2001/56123,2001,A1

[3]Patent:US2002/193348,2002,A1

[4]Patent:EP976722,2000,A1

[5]Patent:EP1065200,2001,A1

[6]JournalofMedicinalChemistry,2013,vol.56,p.8696-8711

1126-09-6

1136-45-4

Ethyl1-(5-methyl-3-phenylisoxazol-4-yl)carbonylpiperidine-4-carboxylate

[1]Patent:US2008/21022,2008,A1.Locationinpatent:Page/Pagecolumn84

Literature

Title: Synthesis, antimicrobial, and anti-inflammatory activities of novel 5-(1-adamantyl)-4-arylideneamino-3-mercapto-1,2,4-triazoles and related derivatives.

Journal: Molecules (Basel, Switzerland) 20100409

Title: Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography.

Journal: Journal of medicinal chemistry 20090813

Title: 4-Pyridyl carbonyl compounds as thrips lures: effectiveness for Western flower thrips in y-tube bioassays.

Journal: Journal of agricultural and food chemistry 20080813

Title: 4-pyridyl carbonyl and related compounds as thrips lures: effectiveness for onion thrips and new zealand flower thrips in field experiments.

Journal: Journal of agricultural and food chemistry 20070725

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SDS