hydron;2-(1,2,3,4-tetrahydronaphthalen-1-yl)-4,5-dihydro-1H-imidazole;chloride

Base Information

• Chemical Name: hydron;2-(1,2,3,4-tetrahydronaphthalen-1-yl)-4,5-dihydro-1H-imidazole;chloride
• CAS No.: 522-48-5
• Molecular Formula: C13H16N2^.HCl
• Molecular Weight: 236.744
• Hs Code.: 2933290000
• Pharos Ligand ID: 89MZKKT49QRT
• Mol file: 522-48-5.mol

Synonyms:

Chemical Property of hydron;2-(1,2,3,4-tetrahydronaphthalen-1-yl)-4,5-dihydro-1H-imidazole;chloride

Chemical Property:

• Appearance/Colour: off-white solid
• Vapor Pressure: 4.8E-06mmHg at 25°C
• Melting Point: 197 °C
• Boiling Point: 393.5 °C at 760 mmHg
• Flash Point: 191.8 °C
• PSA: 24.39000
• LogP: 2.67460
• Storage Temp.: Refrigerator
• Solubility.: H2O: freely soluble
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 236.1080262
• Heavy Atom Count: 16
• Complexity: 259

Purity/Quality:

98.0%-100.5%, ^*data from raw suppliers

Tetrahydrozoline hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi,Xn
• Hazard Codes: Xn,Xi
• Statements: 22-36/37/38
• Safety Statements: 26-36

MSDS Files:

Useful:

• Canonical SMILES: [H+].C1CC(C2=CC=CC=C2C1)C3=NCCN3.[Cl-]
• Uses: An alpha agonist, causing constriction of conjunctival blood vessels. Used in over-the-counter eye drops, this compound relieves the redness left by ocular irritants. 2-Tetralin-1-yl-4,5-dihydro-1H-imidazole hydrochloride is an alpha agonist, causing constriction of conjunctival blood vessels,it is used in over-the-counter eye drops, this compound relieves the redness left by ocular irritants.
• Therapeutic Function: Nasal decongestant, Pharmaceutic aid

Technology Process of hydron;2-(1,2,3,4-tetrahydronaphthalen-1-yl)-4,5-dihydro-1H-imidazole;chloride

There total 5 articles about hydron;2-(1,2,3,4-tetrahydronaphthalen-1-yl)-4,5-dihydro-1H-imidazole;chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ diclofenac sodium (15307-79-6) + tetryzoline hydrochloride (522-48-5)

Guidance literature:

Reference yield:

→ tetryzoline hydrochloride (522-48-5) + [1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid (53-86-1)

Guidance literature:

Reference yield:

→ fluorobiprofen (5104-49-4) + tetryzoline hydrochloride (522-48-5)

Guidance literature:

Refernces

• 1、 -. "Use of combinations comprising non-sedating antihistamines and alpha-adrenergic drugs for the topical treatment of rhinitis/conjunctivitis and cold, cold-like and/or flu symptoms". . . Retrieved 2008/06/13.
• 2、 -. "Pharmaceutical composition for ophthalmic use comprising a nonsteroidal anti-inflammatory and a decongestant drug". . . Retrieved 2008/06/13.