trans-2-Amino-cyclopentanol hydrochloride

Suppliers

Names

[ 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

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)