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1-Boc-4-piperidinemethanol

Names

[ CAS No. ]:
123855-51-6

[ Name ]:
1-Boc-4-piperidinemethanol

[Synonym ]:
1-(tert-Butoxycarbonyl)-4-piperidinemethanol
N-BOC-4-Piperidinemethanol
MFCD02094488
N-tert-Butyloxycarbonyl-4-piperidinemethanol
1-Piperidinecarboxylic acid, 4-(hydroxymethyl)-, 1,1-dimethylethyl ester
1-Boc-4-(hydroxymethyl)piperidine
2-Methyl-2-propanyl 4-(hydroxymethyl)-1-piperidinecarboxylate
1-(tert-Butoxycarbonyl)-4-(hydroxymethyl)piperidine
tert-Butyl-4-(hydroxymethyl)piperidin-1-carboxylat
1-Boc-4-piperidinemethanol
tert-butyl 4-(Hydroxymethyl)piperidine-1-carboxylate
N-(tert-Butoxycarbonyl)-4-piperidinemethanol

Biological Activity

[Description]:

N-Boc-4-piperidinemethanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
308.0±15.0 °C at 760 mmHg

[ Melting Point ]:
78-82 °C(lit.)

[ Molecular Formula ]:
C11H21NO3

[ Molecular Weight ]:
215.29

[ Flash Point ]:
140.1±20.4 °C

[ Exact Mass ]:
215.152145

[ PSA ]:
49.77000

[ LogP ]:
0.88

[ Vapour Pressure ]:
0.0±1.5 mmHg at 25°C

[ Index of Refraction ]:
1.479

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis and pharmacological evaluation of piperidinoalkanoyl-1,2,3,4-tetrahydroisoquinoline derivatives as novel specific bradycardic agents.

Bioorg. Med. Chem. Lett. 14 , 3049-3052, (2004)

A series of piperidinoalkanoyl-1,2,3,4-tetrahydroisoquinoline derivatives were synthesized, and their bradycardic activities were investigated in the isolated right atria of guinea pigs and in conscio...


More Articles


Related Compounds

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