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Key Documents

532169

Sigma-Aldrich

(R)-(−)-N-Boc-3-pyrrolidinol

98%

Synonym(s):

(R)-N-tert-Butoxycarbonyl-(−)-3-pyrrolidinol

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About This Item

Empirical Formula (Hill Notation):
C9H17NO3
CAS Number:
Molecular Weight:
187.24
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

optical activity

[α]20/D −26±1, c = 1 in methanol

mp

62-65 °C (lit.)

SMILES string

CC(C)(C)OC(=O)N1CC[C@@H](O)C1

InChI

1S/C9H17NO3/c1-9(2,3)13-8(12)10-5-4-7(11)6-10/h7,11H,4-6H2,1-3H3/t7-/m1/s1

InChI key

APCBTRDHCDOPNY-SSDOTTSWSA-N

Application

Used in synthesis of ligands for the nicotinic acetylcholine receptor.
Used in the synthesis of anticoagulants.

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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J Lee et al.
Bioorganic & medicinal chemistry letters, 10(10), 1063-1066 (2000-06-08)
The preparation of novel pyridyl ethers as ligands for the nicotinic acetylcholine receptor (nAChR) is described. Variations of the ring size of the azacycle and substitution on the pyridine had dramatic effects on receptor binding affinity with IC50s at the
Satoshi Komoriya et al.
Bioorganic & medicinal chemistry, 12(9), 2099-2114 (2004-04-15)
Since factor Xa (fXa) plays a pivotal role in the blood coagulation cascade, inhibition of fXa is thought to be an effective treatment for a variety of thrombotic events. (2S)-2-[4-[[(3S)-1-Acetimidoyl-3-pyrrolidinyl]oxy]phenyl]-3-(7-amidino-2-naphthyl)propanoic acid hydrochloride pentahydrate (DX-9065a) was previously found in our laboratory

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