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Butaclamol

Base Information Edit
  • Chemical Name:Butaclamol
  • CAS No.:56245-67-1
  • Molecular Formula:C25H31NO
  • Molecular Weight:361.5197
  • Hs Code.:
  • DSSTox Substance ID:DTXSID701317857
  • Nikkaji Number:J78.104E
  • Wikipedia:Butaclamol
  • Wikidata:Q5002336
  • NCI Thesaurus Code:C81088
  • Pharos Ligand ID:4R8DXA591LKU
  • ChEMBL ID:CHEMBL8514
  • Mol file:56245-67-1.mol
Butaclamol

Synonyms:AY 23,028;AY-23,028;AY23,028;Butaclamol;Butaclamol Hydrochloride;Hydrochloride, Butaclamol

Suppliers and Price of Butaclamol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • (+)-BUTACLAMOL 95.00%
  • 5MG
  • $ 498.84
Total 1 raw suppliers
Chemical Property of Butaclamol Edit
Chemical Property:
  • Boiling Point:500.3°Cat760mmHg 
  • PKA:pKa 7.2 (Uncertain) 
  • Flash Point:239.9°C 
  • PSA:23.47000 
  • Density:1.16g/cm3 
  • LogP:4.78270 
  • XLogP3:5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:361.240564612
  • Heavy Atom Count:27
  • Complexity:553
Purity/Quality:

95+% *data from raw suppliers

(+)-BUTACLAMOL 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)C1(CCN2CC3C4=CC=CC=C4CCC5=C3C(=CC=C5)C2C1)O
  • Isomeric SMILES:CC(C)(C)[C@@]1(CCN2C[C@H]3C4=CC=CC=C4CCC5=C3C(=CC=C5)[C@@H]2C1)O
Technology Process of Butaclamol

There total 3 articles about Butaclamol 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:
Guidance literature:
Keton 11b, t-BuLi;
DOI:10.1021/jm00193a004
Guidance literature:
2/Bzl., tert-Butyllithium, Pentan, 0grad;
DOI:10.1021/jm00236a016
Guidance literature:
(CH3)3C-Li, entspr. Keton;
Refernces Edit
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