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3-Methyl-1-adamantaneacetic acid

Base Information
  • Chemical Name:3-Methyl-1-adamantaneacetic acid
  • CAS No.:14202-13-2
  • Molecular Formula:C13H20 O2
  • Molecular Weight:208.301
  • Hs Code.:
  • European Community (EC) Number:238-054-4
  • DSSTox Substance ID:DTXSID40931304
3-Methyl-1-adamantaneacetic acid

Synonyms:3-Methyl-1-adamantaneacetic acid;14202-13-2;2-(3-methyl-1-adamantyl)acetic acid;3-methyladamantan-1-ylacetic acid;EINECS 238-054-4;3-Methyltricyclo(3.3.1.13,7)decan-1-ylacetic acid;(3-methyladamantan-1-yl)acetic acid;3-methyltricyclo[3.3.1.13,7]decan-1-ylacetic acid;CBMicro_019139;Tricyclo(3.3.1.1(3,7)-)decane-1-acetic acid, 3-methyl-;Tricyclo[3.3.1.1(3,7)-]decane-1-acetic acid, 3-methyl-;Cambridge id 5357729;Oprea1_266934;SCHEMBL503339;DTXSID40931304;HMS1608I12;(3-Methyl-1-adamantyl)acetic acid;CCG-7258;(3-Methyl-1-adamantyl)acetic acid #;BIM-0018944.P001;AB00082794-01;SR-01000400504;SR-01000400504-1

Suppliers and Price of 3-Methyl-1-adamantaneacetic acid
Supply Marketing:
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
Total 4 raw suppliers
Chemical Property of 3-Methyl-1-adamantaneacetic acid
Chemical Property:
  • Vapor Pressure:3.62E-05mmHg at 25°C 
  • Boiling Point:328.9°C at 760 mmHg 
  • Flash Point:164.7°C 
  • Density:1.149g/cm3 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:208.146329876
  • Heavy Atom Count:15
  • Complexity:294
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CC3CC(C1)CC(C3)(C2)CC(=O)O
Technology Process of 3-Methyl-1-adamantaneacetic acid

There total 12 articles about 3-Methyl-1-adamantaneacetic acid 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:
1,1-Dichloroethylene; 3-methyl-1-adamantanol; With sulfuric acid; In dichloromethane; at 0 - 30 ℃;
With water; In dichloromethane; at 0 ℃;
DOI:10.1134/S1070428017080024
Guidance literature:
Multi-step reaction with 5 steps
1: H2SO4
2: H2SO4
3: LiAlH4
4: HBr / acetic acid
5: (i) Mg, (ii) /BRN= 1900390/
With lithium aluminium tetrahydride; sulfuric acid; hydrogen bromide; In acetic acid;
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