2,4-Dimethoxybenzylamine - CAS 20781-20-8
Catalog: |
BB016296 |
Product Name: |
2,4-Dimethoxybenzylamine |
CAS: |
20781-20-8 |
Synonyms: |
(2,4-dimethoxyphenyl)methanamine |
IUPAC Name: | (2,4-dimethoxyphenyl)methanamine |
Description: | 2,4-Dimethoxybenzylamine (CAS# 20781-20-8) is a useful research chemical. |
Molecular Weight: | 167.21 |
Molecular Formula: | C9H13NO2 |
Canonical SMILES: | COC1=CC(=C(C=C1)CN)OC |
InChI: | InChI=1S/C9H13NO2/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-5H,6,10H2,1-2H3 |
InChI Key: | QOWBXWFYRXSBAS-UHFFFAOYSA-N |
Boiling Point: | 140 °C |
Purity: | 95 % |
Density: | 1.113 g/cm3 |
Appearance: | Colorless to faint yellow liquid to viscous liquid |
MDL: | MFCD00052393 |
LogP: | 1.86280 |
GHS Hazard Statement: | H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113185534-A | Preparation and application of 2, 4-dimethoxy benzyl urea compound | 20210514 |
CN-113262644-A | Novel high-flux positively-charged nanofiltration membrane and preparation method thereof | 20210428 |
CN-113061349-A | Perylene pigment and preparation method thereof | 20210324 |
CN-112574085-A | Preparation method of 5-amino-2-azaspiro [3.4] octane-2-carboxylic acid tert-butyl ester | 20201218 |
CN-111635334-A | Method for generating nitrile by catalyzing primary amine acceptor-free dehydrogenation through Ru complex | 20200713 |
PMID | Publication Date | Title | Journal |
22893112 | 20121007 | Efficacious N-protection of O-aryl sulfamates with 2,4-dimethoxybenzyl groups | Organic & biomolecular chemistry |
20143822 | 20100305 | Total synthesis of (-)-muraymycin D2 and its epimer | The Journal of organic chemistry |
19456169 | 20090703 | Application of the Ugi reaction for the one-pot synthesis of uracil polyoxin C analogues | The Journal of organic chemistry |
17276683 | 20070401 | N-Hydroxythiosemicarbazones: synthesis and in vitro antitubercular activity | Bioorganic & medicinal chemistry letters |
16677014 | 20060501 | Polymer-supported N-derivatized, o-linked hydroxylamine for concurrent solid-phase synthesis of diverse N-alkyl and N-H hydroxamates | Journal of combinatorial chemistry |
Complexity: | 130 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 167.094628657 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 167.094628657 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 44.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.3 |
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