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129550

Sigma-Aldrich

4-(2-Keto-1-benzimidazolinyl)piperidine

98%

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About This Item

Fórmula empírica (notación de Hill):
C12H15N3O
Número de CAS:
20662-53-7
Peso molecular:
217.27
EC Number:
243-950-3
MDL number:
MFCD00005714
UNSPSC Code:
12352100
PubChem Substance ID:
24847910
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

183-185 °C (lit.)

SMILES string

O=C1Nc2ccccc2N1C3CCNCC3

InChI

1S/C12H15N3O/c16-12-14-10-3-1-2-4-11(10)15(12)9-5-7-13-8-6-9/h1-4,9,13H,5-8H2,(H,14,16)

InChI key

BYNBAMHAURJNTR-UHFFFAOYSA-N

Application

4-(2-Keto-1-benzimidazolinyl)piperidine was used to study the structure–activity relationships with several potent and selective analogues.

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
11729CE
01907DE
S34242
12128MS
11223KI

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Ho Yin Lo et al.
Bioorganic & medicinal chemistry letters, 21(15), 4533-4539 (2011-07-08)
A new class of chymase inhibitor featuring a benzimidazolone core with an acid side chain and a P(1) hydrophobic moiety is described. Incubation of the lead compound with GSH resulted in the formation of a GSH conjugate on the benzothiophene
S M Candura et al.
British journal of pharmacology, 118(8), 1965-1970 (1996-08-01)
1. In strips of human isolated detrusor muscle, the 5-hydroxytryptamine (5-HT) receptor (5-HT4) that mediates facilitation of neuromuscular cholinergic transmission was further characterized by using 5-HT and a series of ligands known for their 5-HT4 agonist (5-methoxytryptamine: 5-MeOT, cisapride, (R,S)-zacopride
Rapid liquid-phase combinatorial synthesis of heterocyclic libraries.
Chung-Ming Sun
Methods in molecular biology (Clifton, N.J.), 201, 141-166 (2002-10-03)
Mike Frohn et al.
Bioorganic & medicinal chemistry letters, 17(23), 6633-6637 (2007-10-09)
We report the development of the novel N-substituted benzimidazole 11 as a potent and selective human formyl peptide receptor-like 1 (hFPRL1) agonist. This compound and its less active enantiomer 12 were identified as useful tools for studying receptor function in
P Zhang et al.
Bioorganic & medicinal chemistry letters, 11(20), 2747-2750 (2001-10-10)
Novel 6-aryl benzimidazolones and benzothiazolones were prepared and examined as bioisosteres of the recently reported 6-aryl dihydroquinolines (1) for progesterone receptor (PR) antagonist activities. PR antagonist activities increased when compounds 9c-f possessed a more lipophilic group at position-1 and pendent
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