Pipenzolate bromide

Base Information

• Chemical Name: Pipenzolate bromide
• CAS No.: 125-51-9
• Molecular Formula: C22H28 N O3 . Br
• Molecular Weight: 434.373
• Hs Code.: 2933399090
• European Community (EC) Number: 204-741-2
• NSC Number: 758221,4347
• UNII: JPX41DUS2B
• DSSTox Substance ID: DTXSID2023480
• Wikipedia: Pipenzolate_bromide
• Wikidata: Q27281629
• NCI Thesaurus Code: C170321
• ChEMBL ID: CHEMBL1401367
• Mol file: 125-51-9.mol

Synonyms:1-ethyl-3-hydroxy-1-methylpiperidinium bromide benzilate;AN 1111;Ila-Med;pipenzolate;pipenzolate bromide;Piptal

Chemical Property of Pipenzolate bromide

Chemical Property:

• Appearance/Colour: White Powder
• Melting Point: 179-180°
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 46.53000
• Density: g/cm³
• LogP: 0.05740
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 433.12526
• Heavy Atom Count: 27
• Complexity: 450

Purity/Quality:

99%, ^*data from raw suppliers

Piptalake ^*data from reagent suppliers

Safty Information:

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

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[N+]1(CCCC(C1)OC(=O)C(C2=CC=CC=C2)(C3=CC=CC=C3)O)C.[Br-]
• Uses: antispasmodic Piptalake is used in the treatment with copper-tolylterpyridine and platinum-tolylterpyridine that targets telomeres and telomerase for regulation of chromosome mis-segregation rates for cancer therapy.
• Therapeutic Function: Spasmolytic

Technology Process of Pipenzolate bromide

There total 1 articles about Pipenzolate bromide 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:

methyl bromide (74-83-9) → pipenzolate bromide (125-51-9)

Guidance literature:

With ethanol;

DOI:10.1021/ja01126a039

upstream raw materials:

methyl bromide