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143900-44-1

143900-44-1 Structure

143900-44-1 Structure
IdentificationMore
[Name]

(S)-1-Boc-3-hydroxypiperidine
[CAS]

143900-44-1
[Synonyms]

1-PIPERIDINECARBOXYLIC ACID, 3-HYDROXY-, 1,1-DIMETHYLETHYL ESTER, (3S)-
(S)-1-BOC-3-HYDROXYPIPERIDINE
(S)-1-BOC-3-PIPERIDINOL
(S)-1-N-BOC-3-HYDROXY-PIPERIDINE
(S)-3-HYDROXY-1-(TERT-BUTOXYCARBONYL)PIPERIDINE
(S)-3-HYDROXY-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(S)-N-BOC-3-HYDROXY PIPERIDINE
(S)-N-(TERT-BUTOXYCARBONYL)-3-HYDROXYPIPERIDINE HYDROCHLORIDE
(S)-TERT BUTYL-3-HYDROXYPIPERIDINE-1-CARBOXYLATE
(S)-1-TERT-BUTOXYCARBONYL-3-HYDROXYPIPERIDINE
(S)-N-tert-Butoxycarbonyl-3-hydroxypiperidine
(S)-3-Hydroxypiperidine, N-BOC protected
(S)-1-BOC-Piperidin-3-ol
[EINECS(EC#)]

1308068-626-2
[Molecular Formula]

C10H19NO3
[MDL Number]

MFCD06659041
[Molecular Weight]

201.26
[MOL File]

143900-44-1.mol
Chemical PropertiesBack Directory
[Melting point ]

34-40 °C
[Boiling point ]

292.3±33.0 °C(Predicted)
[density ]

1.107±0.06 g/cm3(Predicted)
[Fp ]

110 °C
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

Soluble in methanol.
[form ]

Powder or Crystalline Powder
[pka]

14.74±0.20(Predicted)
[color ]

White to tan
[Optical Rotation]

[α]22/D +10.0°, c = 1 in chloroform
[InChI]

InChI=1S/C10H19NO3/c1-10(2,3)14-9(13)11-6-4-5-8(12)7-11/h8,12H,4-7H2,1-3H3/t8-/m0/s1
[InChIKey]

UIJXHKXIOCDSEB-QMMMGPOBSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCC[C@H](O)C1
[CAS DataBase Reference]

143900-44-1(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

(S)-1-Boc-3-hydroxypiperidine is an important chiral intermediate for the synthesis of ibrutinib, an anticancer drug targeting B-cell malignancies. Synthesis of pharmaceutical intermediates including ibrutinib, the API of the newly approved drug Imbruvica, for the treatment of lymphoma.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

3
[REACH Registrations]

Active
[HS Code ]

29333990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Description]

(S)-1-Boc-3-hydroxypiperidine, alias (S)-N-Boc-3-hydroxypiperidine (S-NBHP) is an important chiral intermediate for the synthesis of ibrutinib, an anticancer drug targeting B-cell malignancies.S-NBHP can be prepared in a variety of ways such as chemically or biocatalytically. S-NBHP can be prepared in various ways, such as chemical synthesis or biocatalysis. Biocatalysis is an efficient process for the reduction of N-Boc-piperidin-3-one by recombinant keto reductase (KRED) catalytic to obtain optically pure S-NBHP using 99% yield. The asymmetric reduction of N-Boc-piperidin-3-one (NBPO) to (S)-NBHP can also be catalysed by a reductase (YDR541C) isolated from Saccharomyces cerevisiae in 99% yield.
[Chemical Properties]

White powder
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-1-Boc-3-hydroxypiperidine(143900-44-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

143900-44-1(sigmaaldrich)
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