129550
4-(2-酮酸-1-苯并咪唑)哌啶
98%
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关于此项目
经验公式（希尔记法）:
C12H15N3O
化学文摘社编号:
分子量:
217.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
243-950-3
MDL number:
产品名称
4-(2-酮酸-1-苯并咪唑)哌啶, 98%
InChI key
BYNBAMHAURJNTR-UHFFFAOYSA-N
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)
SMILES string
O=C1Nc2ccccc2N1C3CCNCC3
assay
98%
form
solid
mp
183-185 °C (lit.)
Quality Level
Application
4-(2-Keto-1-benzimidazolinyl)piperidine was used to study the structure–activity relationships with several potent and selective analogues.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Ahmed Kamal et al.
Mini reviews in medicinal chemistry, 6(1), 71-89 (2006-02-07)
Quinoxaline, quinazoline and benzimidazole based templates have been synthesized on solid-support employing different methodologies. This review enlightens academic and industrial examples of combinatorial synthesis for this type of heterocycles that appeared in the literature in the last decade. Hence, some
Jacco van de Streek et al.
Acta crystallographica. Section B, Structural science, 65(Pt 2), 200-211 (2009-03-21)
The crystal structures of six industrially produced benzimidazolone pigments [Pigment Orange 36 (beta phase), Pigment Orange 62, Pigment Yellow 151, Pigment Yellow 154 (alpha phase), Pigment Yellow 181 (beta phase) and Pigment Yellow 194] were determined from laboratory X-ray powder
Brahim Lakhrissi et al.
Carbohydrate research, 343(3), 421-433 (2007-12-25)
New water-soluble benzimidazolone derivatives were synthesized. In the first approach, di-N-glycosyl and mono-N-alkyl-N-glycosyl compounds were obtained by grafting C-6-activated glycosides onto benzimidazolone. In the second approach, benzimidazolone derivatives bearing a glucosyl unit were synthesized using an efficient glycosylation method. Every
P C Pan et al.
Bioorganic & medicinal chemistry letters, 9(11), 1537-1540 (1999-07-01)
A method for soluble, inexpensive polymer-supported synthesis of aryl amines and benzimidazolone on the basis of nucleophilic aryl substitution (S(N)Ar) is described. This method involves a direct coupling reaction between resin bound aryl fluoride and amines at ambient temperature. The
Don R Finley et al.
Bioorganic & medicinal chemistry letters, 16(21), 5691-5694 (2006-08-26)
The synthesis and biological evaluation of a series of benzimidazolone beta(3) adrenergic receptor agonists are described. A trend toward the reduction of rat atrial tachycardia upon increasing steric bulk at the 3-position of the benzimidazolone moiety was observed.
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