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3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride

Base Information
  • Chemical Name:3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride
  • CAS No.:435342-23-7
  • Molecular Formula:C11H15 N O4 . Cl H
  • Molecular Weight:225.2411
  • Hs Code.:
  • Mol file:435342-23-7.mol
3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride

Synonyms:435342-23-7;3-METHYL-5-MORPHOLIN-4-YLMETHYL-FURAN-2-CARBOXYLIC ACID HYDROCHLORIDE;3-methyl-5-(morpholin-4-ylmethyl)furan-2-carboxylic acid;hydrochloride;BIM-0037230.P001;Cambridge id 5921080;AKOS015844382;CS-0365943;3-Methyl-5-(morpholinomethyl)furan-2-carboxylic acid hydrochloride

Suppliers and Price of 3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride
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
  • Matrix Scientific
  • 3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride
  • 1g
  • $ 378.00
  • Crysdot
  • 3-Methyl-5-(morpholinomethyl)furan-2-carboxylicacid 97%
  • 5g
  • $ 701.00
  • American Custom Chemicals Corporation
  • 3-METHYL-5-MORPHOLIN-4-YLMETHYL-FURAN-2-CARBOXYLIC ACID 95.00%
  • 5MG
  • $ 500.40
Total 9 raw suppliers
Chemical Property of 3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride
Chemical Property:
  • Vapor Pressure:6.71E-06mmHg at 25°C 
  • Boiling Point:362.8°Cat760mmHg 
  • Flash Point:173.2°C 
  • PSA:62.91000 
  • Density:1.262g/cm3 
  • LogP:1.05630 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:261.0767857
  • Heavy Atom Count:17
  • Complexity:252
Purity/Quality:

98%min *data from raw suppliers

3-Methyl-5-morpholin-4-ylmethyl-furan-2-carboxylic acid hydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=C(OC(=C1)CN2CCOCC2)C(=O)O.Cl
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