2,4,6-Trimethoxyaniline - CAS 14227-17-9
Catalog: |
BB009337 |
Product Name: |
2,4,6-Trimethoxyaniline |
CAS: |
14227-17-9 |
Synonyms: |
2,4,6-trimethoxyaniline; 2,4,6-trimethoxyaniline |
IUPAC Name: | 2,4,6-trimethoxyaniline |
Description: | 2,4,6-Trimethoxyaniline (CAS# 14227-17-9) is a useful research chemical. |
Molecular Weight: | 183.20 |
Molecular Formula: | C9H13NO3 |
Canonical SMILES: | COC1=CC(=C(C(=C1)OC)N)OC |
InChI: | InChI=1S/C9H13NO3/c1-11-6-4-7(12-2)9(10)8(5-6)13-3/h4-5H,10H2,1-3H3 |
InChI Key: | FNSAKXLEFPFZOM-UHFFFAOYSA-N |
Boiling Point: | 306.9 °C at 760 mmHg |
Density: | 1.118 g/cm3 |
Appearance: | Solid |
MDL: | MFCD00017165 |
LogP: | 1.87580 |
Publication Number | Title | Priority Date |
FR-3094210-A1 | Coloring process using peroxygen salts and a substrate comprising oxidation dyes | 20190329 |
CN-108546233-A | A method of arylamine is prepared by conductor photocatalysis C-H activation | 20180522 |
CN-108546233-B | A method of arylamine is prepared by conductor photocatalysis C-H activation | 20180522 |
EP-3786196-A1 | Method for producing copolymer of allyl monomer having polar group | 20180425 |
US-2021040251-A1 | Method for producing copolymer of allyl monomer having polar group | 20180425 |
PMID | Publication Date | Title | Journal |
19937550 | 20100401 | Minor secondary metabolic products from the stem bark of Plumeria rubra Linn. displaying antimicrobial activities | Planta medica |
Complexity: | 140 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 183.08954328 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 183.08954328 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 53.7 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.2 |
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