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

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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-Carbamoyl-4-methylpyridine-2-carboxylic acid
rac-(5R,6R)-5-amino-1-methyl-6-(1-methyl-1H-imidazol-5-yl)piperidin-2-one
(Z)-3-(1,2,2,3-Tetramethylcyclopentyl)prop-2-enoic acid
(2S,3R)-3-Ethoxy-2-phenylsulfanylcyclobutan-1-one
(2R,4R)-2-Pyridin-2-yloxan-4-amine
(4S,5S)-1-ethyl-4-(hydroxymethyl)-5-(pyridin-3-yl)pyrrolidin-2-one
7-chloro-1,3-dimethyl-1H-pyrazolo[3,4-d]pyridazine
3-(2-Hydroxy-4-(trifluoromethoxy)phenyl)acrylic acid
3-(3,5-dimethyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-4-yl)propanoic acid
rac-benzyl N-[(1R,3S)-3-[(chlorosulfonyl)methyl]cyclopentyl]carbamate

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