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6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE, a compound with the molecular formula C19H30N2O, is a member of the imidazoline receptor agonist class. It is a potential medication that can bind to imidazoline receptors in the body, resulting in physiological effects such as vasoconstriction and reduced release of norepinephrine. This makes it a significant compound in the development of pharmaceuticals for treating cardiovascular and neurological disorders.

769917-29-5

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769917-29-5 Usage

Uses

Used in Pharmaceutical Industry:
6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE is used as a potential medication for treating conditions such as hypertension, nasal congestion, and migraine headaches. Its ability to bind to imidazoline receptors and induce vasoconstriction and reduced release of norepinephrine makes it a valuable compound in the development of pharmaceuticals for cardiovascular and neurological disorders.
Used in Cardiovascular Applications:
6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE is used as a vasoconstrictor for treating hypertension. Its binding to imidazoline receptors leads to vasoconstriction, which helps in lowering blood pressure.
Used in Nasal Congestion Relief:
6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE is used as a decongestant for relieving nasal congestion. Its vasoconstrictive properties help in reducing the swelling of nasal blood vessels, providing relief from nasal congestion.
Used in Migraine Headache Treatment:
6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE is used as a potential treatment for migraine headaches. Its ability to bind to imidazoline receptors and modulate the release of neurotransmitters may help in alleviating the symptoms of migraine headaches.
Used in Neurological Disorders:
6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE is used as a potential medication for treating neurological disorders. Its binding to imidazoline receptors and modulation of neurotransmitter release may have therapeutic effects on various neurological conditions.
Administered through Oral or Nasal Spray:
6-[4-(1H-IMIDAZOL-1-YL)-PHENOXY]-N,N-DIMETHYL-1-HEXANAMINE is typically administered orally or through nasal spray, making it a convenient and effective method of delivery for its therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 769917-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,9,9,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 769917-29:
(8*7)+(7*6)+(6*9)+(5*9)+(4*1)+(3*7)+(2*2)+(1*9)=235
235 % 10 = 5
So 769917-29-5 is a valid CAS Registry Number.

769917-29-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name CAY10434

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:769917-29-5 SDS

769917-29-5Downstream Products

769917-29-5Relevant academic research and scientific papers

Imidazole derivatives as new potent and selective 20-HETE synthase inhibitors

Nakamura, Toshio,Kakinuma, Hiroyuki,Umemiya, Hiroki,Amada, Hideaki,Miyata, Noriyuki,Taniguchi, Kazuo,Bando, Kagumi,Sato, Masakazu

, p. 333 - 336 (2007/10/03)

In a previous paper, we reported that an imidazole derivative 1 exhibited a potent inhibitory activity of 20-HETE synthase (1; IC50 value of 5.7 nM), but this compound also exhibited little selectivity for cytochrome P450s (CYPs). We examined some derivatives of imidazole 1 which had an amino group on the side chain, and found that a dimethylaminohexyloxy derivative (3g; IC50 value of 8.8 nM) showed potent and selective inhibitory activity.

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