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3-Methyl-4-nitrobenzyl alcohol

Base Information
  • Chemical Name:3-Methyl-4-nitrobenzyl alcohol
  • CAS No.:80866-75-7
  • Molecular Formula:C8H9NO3
  • Molecular Weight:167.164
  • Hs Code.:29062990
  • European Community (EC) Number:279-578-3
  • DSSTox Substance ID:DTXSID70230756
  • Nikkaji Number:J149.928I
  • Wikidata:Q83111464
  • Mol file:80866-75-7.mol
3-Methyl-4-nitrobenzyl alcohol

Synonyms:3-Methyl-4-nitrobenzyl alcohol;80866-75-7;(3-Methyl-4-nitrophenyl)methanol;Benzenemethanol, 3-methyl-4-nitro-;EINECS 279-578-3;3-Methyl-4-nitrobenzylalcohol;SCHEMBL713941;4-nitro-3-methylbenzyl alcohol;DTXSID70230756;(3-methyl-4-nitro-phenyl)methanol;(3-Methyl-4-nitro-phenyl)-methanol;(3-Methyl-4-nitrophenyl)methanol #;CL9277;MFCD00007171;AKOS016010481;3-Methyl-4-nitrobenzyl alcohol, 98%;AM804368;AS-46273;CS-0039172;FT-0616092;M2915;EN300-130017;A839989;Z1255386715;3-Methyl-4-nitrobenzyl Alcohol;Benzenemethanol,3-methyl-4-nitro-

Suppliers and Price of 3-Methyl-4-nitrobenzyl alcohol
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
  • Usbiological
  • 3-Methyl-4-nitrobenzyl alcohol
  • 2g
  • $ 343.00
  • TCI Chemical
  • 3-Methyl-4-nitrobenzyl Alcohol >98.0%(GC)
  • 1g
  • $ 37.00
  • TCI Chemical
  • 3-Methyl-4-nitrobenzyl Alcohol >98.0%(GC)
  • 5g
  • $ 112.00
  • Sigma-Aldrich
  • 3-Methyl-4-nitrobenzyl alcohol 98%
  • 10g
  • $ 190.00
  • Frontier Specialty Chemicals
  • 3-Methyl-4-nitrobenzyl Alcohol 98%
  • 1g
  • $ 68.00
  • Frontier Specialty Chemicals
  • 3-Methyl-4-nitrobenzyl Alcohol 98%
  • 5g
  • $ 238.00
  • Crysdot
  • (3-Methyl-4-nitrophenyl)methanol 95+%
  • 100g
  • $ 840.00
  • Crysdot
  • (3-Methyl-4-nitrophenyl)methanol 95+%
  • 25g
  • $ 337.00
  • ChemScene
  • (3-Methyl-4-nitrophenyl)methanol 99.43%
  • 5g
  • $ 68.00
  • ChemScene
  • (3-Methyl-4-nitrophenyl)methanol 99.43%
  • 25g
  • $ 189.00
Total 22 raw suppliers
Chemical Property of 3-Methyl-4-nitrobenzyl alcohol
Chemical Property:
  • Appearance/Colour:yellow to ochre powder 
  • Vapor Pressure:0.000114mmHg at 25°C 
  • Melting Point:57-58 °C(lit.) 
  • Refractive Index:1.585 
  • Boiling Point:322.6 °C at 760 mmHg 
  • PKA:13.62±0.10(Predicted) 
  • Flash Point:145.2 °C 
  • PSA:66.05000 
  • Density:1.272 g/cm3 
  • LogP:1.91870 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • Solubility.:soluble in Methanol 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:167.058243149
  • Heavy Atom Count:12
  • Complexity:166
Purity/Quality:

97% *data from raw suppliers

3-Methyl-4-nitrobenzyl alcohol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1=C(C=CC(=C1)CO)[N+](=O)[O-]
  • Uses 3-Methyl-4-nitrobenzyl alcohol was used as starting reagent in the synthesis of 3-methyl-4-iodophenylalanine.
Technology Process of 3-Methyl-4-nitrobenzyl alcohol

There total 6 articles about 3-Methyl-4-nitrobenzyl alcohol 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 dimethylsulfide borane complex; In tetrahydrofuran; at 0 ℃; for 18h;
DOI:10.1021/jm00078a014
Guidance literature:
2,4-dimethylnitrobenzene; With cerium(IV) oxide; C40H32MnN8; oxygen; acetic acid; at 125 ℃; under 4500.45 Torr;
With water; at 78 ℃; under 3000.3 Torr;
Guidance literature:
With sodium tetrahydroborate; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmcl.2011.05.009
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