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(S)-3-N-Boc-aminopiperidine

(S)-3-N-Boc-aminopiperidine structure

(S)-3-N-Boc-aminopiperidine 

structure
  • CAS No:

    216854-23-8

  • Formula:

    C10H20N2O2

  • Chemical Name:

    (S)-3-N-Boc-aminopiperidine

  • Synonyms:

    (3S)-3-Aminopiperidine, 3-BOC protected 95+%;Alogliptin Impurity 53;(S)-3-amino-N-boc-piperidine;tert-butyl (S)-piperidin-3-ylcarbamate;tert-butyl (R)-piperidin-3-ylcarbamate;Carbamic acid, N-(3S)-3-piperidinyl-, 1,1-dimethylethyl ester;(3S)-3-Aminopiperidine, 3-BOC protected;(S)-tert-butyl piperidin-3-ylcarbamate hydrochloride

  • Categories:

    Flavors and Fragrances  >  Synthetic Fragrances

(S)-3-N-Boc-aminopiperidine Basic Attributes

200.28

200.152477885 g/mol

626-980-5

DTXSID70363795

Characteristics

50.4 Ų

1.02±0.1 g/cm3

122-127°C

304.8±31.0 °C(Predicted)

12.37±0.20

Safety Information

3

37/38-41-36/37/38

26-39-37/39

Xi

|Danger|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 47 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

(S)-3-N-Boc-aminopiperidine Use and Manufacturing

(S)-3-N-Boc-aminopiperidine can be useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens; and alkynylpyrimidine amide derivatives as orally a vailable inhibitors of Tie-2 kinase.

Computed Properties

Molecular Weight:200.28
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:200.152477885
Monoisotopic Mass:200.152477885
Topological Polar Surface Area:50.4
Heavy Atom Count:14
Complexity:199
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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