Cyclobutanol, 3-amino-, hydrochloride (1:1), cis-
Cyclobutanol, 3-amino-, hydrochloride (1:1), cis- Basic information
- Product Name:
- Cyclobutanol, 3-amino-, hydrochloride (1:1), cis-
- Synonyms:
-
- (1s,3s)-3-aMinocyclobutan-1-ol hydrochloride
- cis-3-Aminocyclobutanol hydrochloride - A0711
- CIS-3-AMINOCYCLOBUTANOL HCL
- cis-3-AMinocyclobutanol hydrochloride
- Cyclobutanol, 3-aMino-, hydrochloride, cis-
- Cyclobutanol, 3-amino-, hydrochloride (1:1),cis-
- cis-3-Aminocyclobutan-1-ol hydrochloride
- 3-aminocyclobutan-1-ol hydrochloride, cis
- CAS:
- 1219019-22-3
- MF:
- C4H10ClNO
- MW:
- 123.58
- Mol File:
- 1219019-22-3.mol
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Cyclobutanol, 3-amino-, hydrochloride (1:1), cis- Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder
- color
- White
- InChI
- InChI=1/C4H9NO.ClH/c5-3-1-4(6)2-3;/h3-4,6H,1-2,5H2;1H/t3-,4+;
- InChIKey
- XUMSHCRPQCZRGX-HKTIBRIUNA-N
- SMILES
- N[C@@H]1C[C@H](O)C1.Cl |&1:1,3,r|
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Cyclobutanol, 3-amino-, hydrochloride (1:1), cis- Usage And Synthesis
Synthesis
389890-43-1
1219019-22-3
General procedure for the synthesis of cis-3-aminocyclobutanol hydrochloride from tert-butyl (cis-3-hydroxycyclobutyl)carbamate: tert-butyl (1S,3S)-3-hydroxycyclobutylcarbamate (see Preparation 4A; 187 mg, 1 mmol, 1.0 equiv.) was dissolved in 4N HCl/MeOH solution (15 mL), and the reaction was stirred for 4 hours at room temperature. Upon completion of the reaction, the reaction mixture was concentrated to afford (1S,3S)-3-aminocyclobutanol hydrochloride (120 mg, 0.98 mmol, 98% yield).ESI-MS (M+1): 88 (calculated value C4H9NO: 87).
References
[1] Patent: WO2011/143366, 2011, A1. Location in patent: Page/Page column 144
Cyclobutanol, 3-amino-, hydrochloride (1:1), cis-Supplier
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Cyclobutanol, 3-amino-, hydrochloride (1:1), cis-(1219019-22-3)Related Product Information
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