(S)-3-Aminobutan-1ol

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Products Intro: Product Name:(S)-3-Amino-1-butanol
CAS:61477-39-2
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Products Intro: Product Name:(S)-3-Aminobutan-1ol
CAS:61477-39-2
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Products Intro: Product Name:(S)-3-Aminobutan-1ol
CAS:61477-39-2
Purity:98% Package:5KG;1KG

(S)-3-Aminobutan-1ol manufacturers

  • (S)-3-Aminobutan-1ol
  • (S)-3-Aminobutan-1ol pictures
  • $8.80 / 1KG
  • 2019-08-09
  • CAS:61477-39-2
  • Min. Order: 1KG
  • Purity: 97%-99%
  • Supply Ability: 100kg
(S)-3-Aminobutan-1ol Basic information
Product Name:(S)-3-Aminobutan-1ol
Synonyms:(S)-3-Aminobutan-1ol;1-Fmoc-4-(Cbz-amino)piperidine-4-carboxylic acid;(3S)-3-Amino-1-butanol;(+)-(S)-3-aMinopropan-1-ol;(3S)-3-aminobutan-1-ol;1-Butanol, 3-amino-, (3S)-;(S)-3-Amin-1-butanol;(S)-3-Aminobutan-1-ol - [A10771]
CAS:61477-39-2
MF:C4H11NO
MW:89.14
EINECS:
Product Categories:
Mol File:61477-39-2.mol
(S)-3-Aminobutan-1ol Structure
(S)-3-Aminobutan-1ol Chemical Properties
Boiling point 168℃
density 0.927
Fp 56℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMSO (Slightly), Ethanol (Sparingly). Methanol (Slightly)
form Oil
pka15.00±0.10(Predicted)
color Colourless to Light Yellow
Optical RotationConsistent with structure
Safety Information
RIDADR 2735
HazardClass 8
PackingGroup 
MSDS Information
(S)-3-Aminobutan-1ol Usage And Synthesis
Chemical PropertiesColorless liquid
Uses(S)-3-Aminobutan-1-ol can be used as an intermediate in the preparation of compounds having HIV integrase inhibitory activity.
Synthesis
benzyl (S)-(4-hydroxybutan-2-yl)carbamate

168827-91-6

(S)-3-Aminobutan-1ol

61477-39-2

General procedure for the synthesis of (S)-3-aminobutanol from (S)-benzyl(4-hydroxybutan-2-yl)carbamate: To a 1000 mL round bottom flask was added a solution of (S)-benzyl(4-hydroxybutan-2-yl)carbamate (30 g, 134.4 mmol, 1.00 eq.) in methanol (500 mL), followed by the addition of palladium carbon (3 g, 0.10 equivalent). The reaction mixture was stirred at 25 °C for 12 h under hydrogen atmosphere. Upon completion of the reaction, the solid catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford 11.7 g (92% yield) of (S)-3-aminobutan-1-ol as a colorless oil. The product was confirmed by 1H NMR (300 MHz, DMSO-d6, ppm): δ 4.48 (3H, s), 3.47 (2H, s), 2.96 (1H, s), 1.47-1.41 (2H, q), 1.02-0.99 (3H, d); the LCMS (ESI) analysis showed a m/z of 90 [M + H]+; the specific spectroscopy measurement value of [α]D22 +11.65° (c = 1.22 g/100 mL in EtOH) is consistent with the literature value of [α]D20 +16.3° (c = 4.5 in EtOH) (J. Org. Chem. 1996, 61, 2293-2304).

References[1] Patent: WO2014/9447, 2014, A1. Location in patent: Page/Page column 96; 97
[2] Patent: WO2014/202741, 2014, A1. Location in patent: Page/Page column 42; 43
[3] Patent: US2015/197529, 2015, A1. Location in patent: Paragraph 1201; 1204
[4] Patent: US2016/168141, 2016, A1. Location in patent: Paragraph 1210; 1213
[5] Patent: WO2016/96936, 2016, A1. Location in patent: Page/Page column 43
Tag:(S)-3-Aminobutan-1ol(61477-39-2) Related Product Information
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