Skip to Content
Merck
All Photos(1)

Documents

644064

Sigma-Aldrich

(R)-(+)-1-Boc-3-aminopyrrolidine

97%

Synonym(s):

(R)-(+)-N-Boc-3-aminopyrrolidine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H18N2O2
CAS Number:
Molecular Weight:
186.25
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.472 (lit.)

bp

243-244 °C (lit.)

density

1.098 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C9H18N2O2/c1-9(2,3)13-8(12)11-5-4-7(10)6-11/h7H,4-6,10H2,1-3H3/t7-/m1/s1

InChI key

CMIBWIAICVBURI-SSDOTTSWSA-N

Looking for similar products? Visit Product Comparison Guide

Application

(R)-(+)-1-Boc-3-aminopyrrolidine may be used to prepare:
  • Descarboxamide analog and Na-methylated analogs of 4-N-(Nω-nitro-L-argininyl)-trans-4-amino-L-proline amide.
  • Histamine 3 (H3) receptor antagonists containing pyrrolidin-3-yl-N-methylbenzamide moiety.

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1

Supplementary Hazards

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

196.0 °F - closed cup

Flash Point(C)

91.1 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Selective l-nitroargininylaminopyrrolidine and L-nitroargininylaminopiperidine neuronal nitric oxide synthase inhibitors.
Seo J, et al.
Bioorganic & Medicinal Chemistry, 15(5), 1928-1938 (2007)
Pyrrolidin-3-yl-N-methylbenzamides as potent histamine 3 receptor antagonists.
Zhou D, et al.
Bioorganic & Medicinal Chemistry Letters, 21(19), 5957-5960 (2011)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service