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

Suppliers

Names

[ Name ]:
4-(Piperidin-4-yl)butanoic acid hydrochloride

[Synonym ]:
4-(4-Piperidinyl)butanoic acid hydrochloride (1:1)
MFCD02684340
4-(Piperidin-4-yl)butanoic acid hydrochloride (1:1)
4-Piperidinebutanoic acid, hydrochloride (1:1)
4-piperidin-4-ylbutanoic acid,hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
344.3ºC at 760 mmHg

[ Melting Point ]:
113-117ºC(lit.)

[ Molecular Formula ]:
C₉H₁₈ClNO₂

[ Molecular Weight ]:
207.698

[ Flash Point ]:
99ºC

[ Exact Mass ]:
207.102600

[ PSA ]:
49.33000

[ LogP ]:
2.37170

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

Articles

Synthesis and biological evaluation of isosteric analogues of FK866, an inhibitor of NAD salvage.

ChemMedChem 3 , 771-779, (2008)

One of the great challenges of medicinal chemistry is to create novel, effective, chemotherapeutic agents that show specificity for cancer cells combined with low systemic toxicity. A novel idea is to...

Design, synthesis and X-ray crystallographic study of NAmPRTase inhibitors as anti-cancer agents.

Eur. J. Med. Chem. 46 , 1153-1164, (2011)

NAmPRTase (PBEF/Visfatin) plays a pivotal role in the salvage pathway of NAD(+) biosynthesis. NAmPRTase has been an attractive target for anti-cancer agents that induce apoptosis of tumor cells via a ...

Characterization of NAD uptake in mammalian cells. Billington RA, et al.

J. Biol. Chem. 283(10) , 6367-6374, (2008)

4-(PIPERIDIN-4-YL)BUTANOIC ACID
4-(Piperidin-4-yl)benzoic acid hydrochloride
4-(2-methylpiperidin-4-yl)butanoic acid,hydrochloride
4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl) butanoic acid hydrochloride
N-Boc-4-Piperidin-4-yl-butyric acid
1-[(1,1-dimethylethoxy)carbonyl]-4-(methoxycarbonyl)-4-piperidinebutanoic acid
5-chloro-N-((1-hydroxy-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)thiophene-2-carboxamide
2-[2-(2-Fluorophenyl)-1,3-thiazol-4-yl]-2-methylpropanoic acid
N-((1-hydroxy-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)-1-naphthamide
2-chloro-6-fluoro-N-((1-hydroxy-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)benzamide
3-Carboxypropyl Hexadecanoate
5-(furan-2-yl)-N-((1-hydroxy-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)isoxazole-3-carboxamide
N-((1-hydroxy-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)benzo[d]thiazole-2-carboxamide
1-Methyl-3-(1H-1,2,3-triazol-4-YL)-1H-pyrazol-5-amine
8-Ethyl-1-thia-4-azaspiro[4.5]decane
Methyl 4-(((1-hydroxy-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)methyl)carbamoyl)benzoate

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