CAMYLOFINE DIHYDROCHLORIDE

Base Information

• Chemical Name: CAMYLOFINE DIHYDROCHLORIDE
• CAS No.: 54-30-8
• Molecular Formula: C19H32 N2 O2
• Molecular Weight: 320.475
• Hs Code.: 2922499990
• European Community (EC) Number: 200-202-0
• UNII: 340B6Q764V
• DSSTox Substance ID: DTXSID7046415
• Nikkaji Number: J38.359G
• Wikipedia: Camylofin
• Wikidata: Q4725854
• NCI Thesaurus Code: C166637
• Metabolomics Workbench ID: 144340
• ChEMBL ID: CHEMBL253592
• Mol file: 54-30-8.mol

Synonyms:Glycine,N-[2-(diethylamino)ethyl]-2-phenyl-, isopentyl ester (6CI,7CI,8CI); Acamylophenine;Adopon; Avacan; Avadyl; Avocan; Belosin; Camylofin; Camylofine; Isoamyl N-(b-diethylaminoethyl)-a-aminophenylacetate; Isoamyl a-[(b-diethylaminoethyl)amino]phenylacetate;N-(2-Diethylaminoethyl)-2-phenylglycine isopentyl ester; Navadyl; Novospasmin;Sintespasmil; Spasmocan; a-[(b-Diethylaminoethyl)amino]phenylaceticacid isoamyl ester

Chemical Property of CAMYLOFINE DIHYDROCHLORIDE

Chemical Property:

• Vapor Pressure: 7.03E-07mmHg at 25°C
• Melting Point: 25°C
• Refractive Index: 1.5020 (estimate)
• Boiling Point: 408.4°Cat760mmHg
• PKA: 10.02±0.25(Predicted)
• Flash Point: 200.8°C
• PSA: 41.57000
• Density: 0.987g/cm³
• LogP: 5.24330
• XLogP3: 3.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 12
• Exact Mass: 320.246378268
• Heavy Atom Count: 23
• Complexity: 311

Purity/Quality:

99%, ^*data from raw suppliers

Camylofine dihydrochloride analytical standard, for drug analysis ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCN(CC)CCNC(C1=CC=CC=C1)C(=O)OCCC(C)C
• Uses: anticholinergic

Technology Process of CAMYLOFINE DIHYDROCHLORIDE

There total 4 articles about CAMYLOFINE DIHYDROCHLORIDE 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:

amino-phenyl-acetic acid isopentyl ester (84580-27-8) + 2-chloro-N,N-diethylethylamine hydrochloride (869-24-9) → Acamylophenine (54-30-8)

Guidance literature:

Reference yield:

N,N-diethylethylenediamine (100-36-7) + 2-Bromo-5-methyl-hexanoic acid phenyl ester → Acamylophenine (54-30-8)

Guidance literature:

DOI:10.1111/j.2042-7158.1960.tb12650.x

Reference yield:

N,N-diethylethylenediamine (100-36-7) → Acamylophenine (54-30-8)

Guidance literature:

upstream raw materials:

amino-phenyl-acetic acid isopentyl ester

2-chloro-N,N-diethylethylamine hydrochloride

N,N-diethylethylenediamine

Downstream raw materials:

i-Amyl alcohol

triethylamine

phenylglycin

Refernces