trans-2-Amino-cyclopentanol hydrochloride

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Names

[ CAS No. ]:
31775-67-4

[ Name ]:
trans-2-Amino-cyclopentanol hydrochloride

[Synonym ]:
Trans-(-)-2-aminocyclopentanol hydrochloride
(1R,2R)-2-Aminocyclopentanol hydrochloride (1:1)
trans-2-Amino-cyclopentanol hydrochloride
(1R,2R)-2-Aminocyclopentanol hydrochloride
trans-2-Aminocyclopentanol hydrochloride
Cyclopentanol, 2-amino-, (1R,2R)-, hydrochloride (1:1)
trans-2-amino-1-cyclopentanol hydrochloride
MFCD02683551
(1R,2R)-rel-2-Aminocyclopentanol hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
220.9ºC at 760 mmHg

[ Melting Point ]:
191-196ºC

[ Molecular Formula ]:
C5H12ClNO

[ Molecular Weight ]:
137.608

[ Flash Point ]:
87.4ºC

[ Exact Mass ]:
137.060745

[ PSA ]:
46.25000

[ LogP ]:
1.36080

Safety Information

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

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922199090

Precursor & DownStream

Precursor

  • (+/-)-trans-2-aminocyclopentanol

DownStream

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

A practical method for the synthesis of highly enantioenriched trans-1,2-amino alcohols.

Org. Lett. 15(12) , 2895-7, (2013)

A highly enantioselective addition of phenyl carbamate to meso-epoxides has been developed to efficiently generate protected trans-1,2-amino alcohols. This transformation is promoted by an oligomeric ...

Stereochemistry of Aminocyclanols. Synthesis of cis Epimers via Oxazolines. The 2-Aminocyclopentanols*. McCasland GE and Smith DA.

J. Am. Chem. Soc. 72(5) , 2190-2195, (1950)

Preparation of antidotes for anticholinesterase poisoning. IV. Synthesis and protective effectiveness of 2'-(cis-and trans-2'-hydroxycyclohexyl) aminoethyl 1-phenylcyclopentanecarboxylate hydrochlorides. Bannard RAB and Parkkari JH.

Can. J. Chem. 48(9) , 1377-1382, (1970)


More Articles


Related Compounds

  • trans-2-Amino-cyclopentanol hydrochloride
  • trans-2-Amino-cyclopentanol hydrochloride
  • trans-2-Amino-cyclopentanol hydrochloride
  • trans-2-Amino-cyclopentanol hydrochloride
  • (1R,2R)-2-Aminocyclopentanol
  • cis-2-Aminocyclopentan-1-ol
  • Ethyl 6-(2-methylpiperidin-4-yl)piperidine-3-carboxylate
  • [4-(2-Methylpiperidin-4-yl)piperidin-2-yl]methanamine
  • 2,2-Diethyl-4,6,6-trimethyl-1,3-oxazinane
  • 2-Amino-4-hydroxy-4,5-dimethylhexanamide
  • 5-butyl-4-chloro-1-methyl-1H-pyrazole
  • (Z)-3-butyl-N'-hydroxyfuran-2-carboximidamide
  • (1-{[(5-Chlorofuran-2-yl)methyl]sulfanyl}pentan-2-yl)(methyl)amine
  • 3-{1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclopentaneamido}oxolane-2-carboxylic acid
  • 3-chloro-6-methyl-4-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]pyridazine
  • 2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methyl-N-(propan-2-yl)but-2-enamido]acetic acid
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