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2-Hydroxypropyl benzoate

Base Information
  • Chemical Name:2-Hydroxypropyl benzoate
  • CAS No.:37086-84-3
  • Deprecated CAS:106565-46-2
  • Molecular Formula:C10H12 O3
  • Molecular Weight:180.203
  • Hs Code.:
  • European Community (EC) Number:253-340-9
  • NSC Number:409885
  • UNII:K4K90ZQ89N
  • DSSTox Substance ID:DTXSID5041229
  • Nikkaji Number:J260.735B
  • Wikidata:Q27281956
  • RXCUI:1797116
  • Mol file:37086-84-3.mol
2-Hydroxypropyl benzoate

Synonyms:2-Hydroxypropyl benzoate;37086-84-3;1,2-Propanediol, 1-benzoate;Propylene glycol monobenzoate;1,2-Propane glycol monobenzoate;UNII-K4K90ZQ89N;K4K90ZQ89N;EINECS 253-340-9;NSC 409885;NSC-409885;AI3-06528;2-hydroxy-1-propyl benzoate;1, 1-benzoate;1-benzoate1,2-propanediol;1,2-Propanediol 1-benzoate;1,2-propanediol monobenzoate;SCHEMBL524376;DTXSID5041229;benzoic acid 2-hydroxy-propyl ester;NSC409885;AS-58106;J260.735B;D93462;Q27281956

Suppliers and Price of 2-Hydroxypropyl benzoate
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 9 raw suppliers
Chemical Property of 2-Hydroxypropyl benzoate
Chemical Property:
  • Vapor Pressure:0.000701mmHg at 25°C 
  • Boiling Point:295.2°C at 760 mmHg 
  • Flash Point:125.1°C 
  • PSA:46.53000 
  • Density:1.138g/cm3 
  • LogP:1.22420 
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:180.078644241
  • Heavy Atom Count:13
  • Complexity:162
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(COC(=O)C1=CC=CC=C1)O
Technology Process of 2-Hydroxypropyl benzoate

There total 28 articles about 2-Hydroxypropyl benzoate 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:
With 2-Aminoethoxydiphenylborane; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 23 ℃; for 4h; regioselective reaction; Inert atmosphere;
DOI:10.1021/ja302549c
Guidance literature:
With methyl magnesium iodide; In diethyl ether; at 0 ℃; for 2h;
DOI:10.1039/c39920000681
Guidance literature:
With tetrabutylammomium bromide; In acetonitrile; for 4h; Heating;
DOI:10.1055/s-2003-42416
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