4-(Piperidin-1-yl)butanoic acid hydrochloride

Base Information

• Chemical Name: 4-(Piperidin-1-yl)butanoic acid hydrochloride
• CAS No.: 5463-76-3
• Molecular Formula: C9H17NO2
• Molecular Weight: 207.7
• Hs Code.: 2933399090
• European Community (EC) Number: 837-635-5
• ChEMBL ID: CHEMBL2001526
• NSC Number: 15135
• Mol file: 5463-76-3.mol

Synonyms:5463-76-3;4-(piperidin-1-yl)butanoic acid hydrochloride;4-piperidin-1-ylbutanoic acid;hydrochloride;4-(1-Piperidinyl)butanoic acid hydrochloride;PIPERIDIN-1-YLBUTANOIC ACID HYDROCHLORIDE;4-Piperidin-1-yl-butyric acid hydrochloride;4-piperidin-1-ylbutyric acid hydrochloride;NSC15135;NSC-15135;4-Piperidin-1-yl-butyric acid;SCHEMBL1127792;CHEMBL2001526;TQP0306;IZVIJYFRXDQEOR-UHFFFAOYSA-N;4-(1-Piperidinyl)butanoic Acid HCl;MFCD06801215;4-Piperidinobutyric acid hydrochloride;AKOS000277621;gamma-piperidinobutyric acid hydrochloride;4-(piperidin-1-yl)butanoicacidhydrochloride;4-piperidin-1-ylbutanoic acid hydrochloride;CS-0250113;EN300-49763;G29935;Z600397690

Chemical Property of 4-(Piperidin-1-yl)butanoic acid hydrochloride

Chemical Property:

• Vapor Pressure: 0.000169mmHg at 25°C
• Boiling Point: 306.9°Cat760mmHg
• Flash Point: 139.4°C
• PSA: 40.54000
• Density: 1.052g/cm³
• LogP: 2.07700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 207.1026065
• Heavy Atom Count: 13
• Complexity: 142

Purity/Quality:

98%min ^*data from raw suppliers

4-(piperidin-1-yl)butanoicAcidhydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(CC1)CCCC(=O)O.Cl

Technology Process of 4-(Piperidin-1-yl)butanoic acid hydrochloride

There total 6 articles about 4-(Piperidin-1-yl)butanoic acid hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

(piperidinyl-1)-4 butanoate d'ethyle (116885-98-4) → γ-piperidinobutyric acid hydrochloride (5463-76-3)

Guidance literature:

With hydrogenchloride; In water; for 1.5h; Reflux;

DOI:10.1016/j.bmcl.2013.09.052

Reference yield:

piperidine (110-89-4) → γ-piperidinobutyric acid hydrochloride (5463-76-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: toluene / 10 h / Reflux

2.1: sodium hydroxide; water / 16 h / Reflux

2.2: 0 °C

With water; sodium hydroxide; In toluene;

DOI:10.1021/jm3013568

Reference yield:

piperidine (110-89-4) → γ-piperidinobutyric acid hydrochloride (5463-76-3)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether

2: aq. HCl / 8 h / Heating

With hydrogenchloride; In diethyl ether; 1: Alkylation / 2: Hydrolysis;

upstream raw materials:

(piperidinyl-1)-4 butanoate d'ethyle

piperidine

1,4-oxazepane

Ethyl 4-bromobutyrate

Downstream raw materials:

4-piperidin-1-yl-butan-1-ol

4-acetamidophenyl 4-(piperidin-1-yl)butanoate hydrochloride

4-acetamidophenyl 4-(piperidin-1-yl)butanoate

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