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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:
109431-87-0
Molecular Weight:
187.24
MDL number:
MFCD01317838
UNSPSC Code:
12352005
PubChem Substance ID:
24877863
NACRES:
NA.22

Quality Level

100

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

Related Categories

Application

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

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H335,H400

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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