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Des(pyrrolidinyl)diethylamino ormeloxifene

Base Information
  • Chemical Name:Des(pyrrolidinyl)diethylamino ormeloxifene
  • CAS No.:78994-27-1
  • Molecular Formula:C30H37NO3
  • Molecular Weight:459.629
  • Hs Code.:
  • UNII:ACK63NL9ZV
Des(pyrrolidinyl)diethylamino ormeloxifene

Synonyms:ACK63NL9ZV;Des(pyrrolidinyl)diethylamino ormeloxifene;UNII-ACK63NL9ZV;Des(pyrrolidinyl) diethylamino centchroman;Des(pyrrolidinyl) diethylamino centchroman, (+/-)-;78994-27-1;Ethanamine, 2-(4-(3,4-dihydro-7-methoxy-2,2-dimethyl-3-phenyl-2H-1-benzopyran-4-yl)phenoxy)-N,N-diethyl-, trans-;N,N-Diethyl-2-(4-((3R,4R)-7-methoxy-2,2-dimethyl-3-phenyl-3,4-dihydrochromen-4-yl)phenoxy)ethanamine

Suppliers and Price of Des(pyrrolidinyl)diethylamino ormeloxifene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of Des(pyrrolidinyl)diethylamino ormeloxifene
Chemical Property:
  • XLogP3:6.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:9
  • Exact Mass:459.27734404
  • Heavy Atom Count:34
  • Complexity:592
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCN(CC)CCOC1=CC=C(C=C1)C2C(C(OC3=C2C=CC(=C3)OC)(C)C)C4=CC=CC=C4
  • Isomeric SMILES:CCN(CC)CCOC1=CC=C(C=C1)[C@H]2[C@@H](C(OC3=C2C=CC(=C3)OC)(C)C)C4=CC=CC=C4
Technology Process of Des(pyrrolidinyl)diethylamino ormeloxifene

There total 4 articles about Des(pyrrolidinyl)diethylamino ormeloxifene 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:
Multi-step reaction with 4 steps
1: 80 percent / K2CO3 / acetone / 35 h / Heating
2: 95 percent / n-BuLi / hexane; dimethylsulfoxide / 16 h / Ambient temperature
3: 93 percent / H2 / Raney Ni / methanol / 8 h / 3102.9 Torr
4: K2CO3 / acetone / 14 h / Heating
With n-butyllithium; hydrogen; potassium carbonate; nickel; In methanol; hexane; dimethyl sulfoxide; acetone;
DOI:10.1021/jm00358a026
Guidance literature:
Multi-step reaction with 3 steps
1: 95 percent / n-BuLi / hexane; dimethylsulfoxide / 16 h / Ambient temperature
2: 93 percent / H2 / Raney Ni / methanol / 8 h / 3102.9 Torr
3: K2CO3 / acetone / 14 h / Heating
With n-butyllithium; hydrogen; potassium carbonate; nickel; In methanol; hexane; dimethyl sulfoxide; acetone;
DOI:10.1021/jm00358a026
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / H2 / Raney Ni / methanol / 8 h / 3102.9 Torr
2: K2CO3 / acetone / 14 h / Heating
With hydrogen; potassium carbonate; nickel; In methanol; acetone;
DOI:10.1021/jm00358a026
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