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3-Methoxybenzylamine

Base Information
  • Chemical Name:3-Methoxybenzylamine
  • CAS No.:5071-96-5
  • Molecular Formula:C8H11NO
  • Molecular Weight:137.181
  • Hs Code.:29222990
  • European Community (EC) Number:225-779-6
  • NSC Number:162042
  • DSSTox Substance ID:DTXSID10198765
  • Nikkaji Number:J41.839K
  • Wikidata:Q27465601
  • ChEMBL ID:CHEMBL468622
  • Mol file:5071-96-5.mol
3-Methoxybenzylamine

Synonyms:3-Methoxybenzylamine;5071-96-5;m-Methoxybenzylamine;(3-Methoxyphenyl)methanamine;Benzenemethanamine, 3-methoxy-;1-(3-methoxyphenyl)methanamine;3-methoxybenzyl amine;MFCD00008115;BENZYLAMINE, m-METHOXY-;(3-methoxybenzyl)amine;EINECS 225-779-6;NSC 162042;BRN 1447182;Benzenemethanamine, 3-methoxy- (9CI);4-13-00-01704 (Beilstein Handbook Reference);(3-methoxyphenyl)methylamine;SZ4;NSC162042;3-methoxylbenzylamine;m-Methoxy Benzylamine;3-methoxy benzylamine;3-methoxy-benzylamine;3-methoxybenzyl-amine;3-methoxy-benzyl amine;C(N)c1cccc(OC)c1;3-Methoxybenzylamine 98+%;3-Methoxybenzylamine, 98%;SCHEMBL42954;(3-methoxyphenyl) methanamine;CHEMBL468622;(3-Methoxyphenyl)methanamine #;DTXSID10198765;BCP11237;1-[3-(methyloxy)phenyl]methanamine;CK2410;STL302642;AKOS000120877;CS-W007351;NSC-162042;PS-6100;SB75376;AC-25955;LS-43381;SY004059;A7488;AM20050130;FT-0615995;M0851;EN300-16224;A19834;Q27465601;3-methoxy-benzenemethanamin;F2190-0493

Suppliers and Price of 3-Methoxybenzylamine
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
  • TRC
  • 3-Methoxybenzylamine
  • 25g
  • $ 1100.00
  • TCI Chemical
  • 3-Methoxybenzylamine >98.0%(GC)(T)
  • 25mL
  • $ 56.00
  • TCI Chemical
  • 3-Methoxybenzylamine >98.0%(GC)(T)
  • 5mL
  • $ 20.00
  • SynQuest Laboratories
  • 3-Methoxybenzylamine 97%
  • 5 g
  • $ 16.00
  • Sigma-Aldrich
  • 3-Methoxybenzylamine 98%
  • 5g
  • $ 79.40
  • Sigma-Aldrich
  • 3-Methoxybenzylamine 98%
  • 1g
  • $ 43.70
  • Medical Isotopes, Inc.
  • 3-Methoxybenzylamine
  • 2.5 g
  • $ 625.00
  • Medical Isotopes, Inc.
  • 3-Methoxybenzylamine
  • 25 g
  • $ 2000.00
  • Matrix Scientific
  • 3-Methoxybenzylamine 95+%
  • 5g
  • $ 47.00
  • Matrix Scientific
  • 3-Methoxybenzylamine 95+%
  • 10g
  • $ 71.00
Total 102 raw suppliers
Chemical Property of 3-Methoxybenzylamine
Chemical Property:
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:0.0428mmHg at 25°C 
  • Refractive Index:n20/D 1.547(lit.)  
  • Boiling Point:238.3 °C at 760 mmHg 
  • PKA:9.03±0.10(Predicted) 
  • Flash Point:98.4 °C 
  • PSA:35.25000 
  • Density:1.028 g/cm3 
  • LogP:1.85420 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C 
  • Sensitive.:Air Sensitive 
  • Water Solubility.:Slightly soluble in water. 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:137.084063974
  • Heavy Atom Count:10
  • Complexity:95.3
Purity/Quality:

99% min *data from raw suppliers

3-Methoxybenzylamine *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi,Corrosive
  • Hazard Codes:Xi,C,Xn 
  • Statements: 36/37/38-20/21/22-22 
  • Safety Statements: 26-36-45-36/37/39 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:COC1=CC=CC(=C1)CN
  • Uses 3-Methoxybenzylamine is a 3-methoxy derivative of benzylamine. 3-Methoxybenzylamine is one the the metabolites detected in urine after metabolism of dopamine analogues. 3-Methoxybenzylamine showed pla smin inhibitory activity as well as weak inhibition of the essential bacterial cell division protein FtsZ 3-Methoxybenzylamine was used in the preparation of 6-substituted purines.
Technology Process of 3-Methoxybenzylamine

There total 20 articles about 3-Methoxybenzylamine 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 sulfuric acid; In various solvent(s); at 20 ℃; for 20h;
DOI:10.1016/S0040-4039(00)01203-X
Guidance literature:
With aluminum oxide; potassium hydroxide; hydrazine; In neat (no solvent); for 1h; Milling;
DOI:10.1039/c8nj04240c
Guidance literature:
With ammonia borane; In methanol; at 50 ℃; for 12h; Inert atmosphere;
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