5-(2-naphthalen-2-yloxyethyl)-1H-imidazole

Modify Date: 2026-08-03 11:51:05

5-(2-naphthalen-2-yloxyethyl)-1H-imidazole Structure
5-(2-naphthalen-2-yloxyethyl)-1H-imidazole structure
Common Name 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole
CAS Number 7728-79-2 Molecular Weight 238.28400
Density 1.213g/cm3 Boiling Point 511.9ºC at 760 mmHg
Molecular Formula C15H14N2O Melting Point N/A
MSDS N/A Flash Point 181.2ºC

 Names

This table lists Chinese names, IUPAC names and various aliases of this chemical substance.

Name 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole
Synonym More Synonyms

 Chemical & Physical Properties

This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.

Density 1.213g/cm3
Boiling Point 511.9ºC at 760 mmHg
Molecular Formula C15H14N2O
Molecular Weight 238.28400
Flash Point 181.2ºC
Exact Mass 238.11100
PSA 37.91000
LogP 3.18440
Index of Refraction 1.659
InChIKey PGMKRSXAILDXTQ-UHFFFAOYSA-N
SMILES c1ccc2cc(OCCc3cnc[nH]3)ccc2c1

 Synthetic Route

This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.

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5-(2-naphthalen-2-yloxyethyl)-1H-imidazole Structure

5-(2-naphthalen...

CAS#:7728-79-2

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Literature: Ganellin, C. Robin; Fkyerat, Abdellatif; Bang-Andersen, Benny; Athmani, Salah; Tertiuk, Wasyl; Garbarg, Monique; Ligneau, Xavier; Schwartz, Jean-Charles Journal of Medicinal Chemistry, 1996 , vol. 39, # 19 p. 3806 - 3813

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5-(2-naphthalen-2-yloxyethyl)-1H-imidazole Structure

5-(2-naphthalen...

CAS#:7728-79-2

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Literature: Huebner et al. Journal of the American Chemical Society, 1949 , vol. 71, p. 3942

 Precursor & DownStream

This table lists upstream starting materials and downstream derivative products related to this chemical.

Precursor  3

DownStream  0

 Bioassay

View more

This table contains target information, in‑vitro & in‑vivo assay data for this compound.

Name: In vivo evaluation for effect on brain tele-methylhistamine levels in mice
Source: ChEMBL
Target: Mus musculus
External Id: CHEMBL732166
Name: Rat Histamine H3 receptor antagonism determined by [K+] - evoked depolarization-induc...
Source: ChEMBL
Target: Histamine H3 receptor
External Id: CHEMBL698419
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 Synonyms

This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.

su-435

  | FAQ

This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.

Q: What is the molecular weight of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: Molecular weight of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is 238.28400.
Q: What is the Chinese name of 7728-79-2?
A: Chinese name of 7728-79-2 is 7728-79-2.
Q: What is the CAS number of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: CAS number of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is 7728-79-2.
Q: What is the InChIKey of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: InChIKey of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is PGMKRSXAILDXTQ-UHFFFAOYSA-N.
Q: What English synonyms does 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole have?
A: English synonyms of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole: su-435.
Q: What is the molecular formula of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: Molecular formula of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is C15H14N2O.
Q: What is the LogP of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: LogP of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is 3.18440.
Q: What is the polar surface area (PSA) of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: Polar surface area (PSA) of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is 37.91000.
Q: What are the upstream materials of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: Related upstream materials(CAS) of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole: 6429-10-3;135-19-3;875-83-2.
Q: What is the SMILES notation of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole?
A: SMILES notation of 5-(2-naphthalen-2-yloxyethyl)-1H-imidazole is c1ccc2cc(OCCc3cnc[nH]3)ccc2c1.
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