3,4-Dimethoxycinnamic acid, predominantly trans - CAS 2316-26-9
Catalog: |
BB017962 |
Product Name: |
3,4-Dimethoxycinnamic acid, predominantly trans |
CAS: |
2316-26-9 |
Synonyms: |
(E)-3-(3,4-dimethoxyphenyl)prop-2-enoic acid |
Application: |
3,4-Dimethoxycinnamic Acid is a Cinnamic Acid (C442030) derivative,used in the synthesis of amides and esters through coupling reactions involving carboxylic acids and amines and N-methylation of amides and O-methylation of carboxylic acids. |
IUPAC Name: | (E)-3-(3,4-dimethoxyphenyl)prop-2-enoic acid |
Description: | 3,4-Dimethoxycinnamic acid isolated from the leaves of Phyllostachys heterocycla. |
Molecular Weight: | 208.21 |
Molecular Formula: | C11H12O4 |
Canonical SMILES: | COC1=C(C=C(C=C1)C=CC(=O)O)OC |
InChI: | InChI=1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)/b6-4+ |
InChI Key: | HJBWJAPEBGSQPR-GQCTYLIASA-N |
Boiling Point: | 367.4 °C at 760 mmHg |
Melting Point: | 181-183°C(lit.) |
Flash Point: | 144.0±17.2 °C |
Purity: | 98.5 % |
Density: | 1.203 g/cm3 |
Solubility: | In Vitro: DMSO : 50 mg/mL(240.14 mM;Need ultrasonic) In Vivo: 1.Add each solvent one by one:10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline Solubility: ≥ 2.5 mg/mL (4.84 mM); Clear solution 2.Add each solvent one by one:10% DMSO >> 90% (20% SBE-β-CD in saline) Solubility: ≥ 2.5 mg/mL (4.84 mM); Clear solution 3.Add each solvent one by one:10% DMSO >> 90% corn oil Solubility: ≥ 2.5 mg/mL (4.84 mM); Clear solution |
Appearance: | White powder |
Storage: | Powder: -20°C: 3 years 4°C: 2 years In solvent: -80°C: 6 months -20°C: 1 month |
MDL: | MFCD00004387 |
LogP: | 1.80160 |
Quality Standard: | Enterprise Standard |
Vapor Pressure: | 0.0±0.9 mmHg at 25°C |
GHS Hazard Statement: | H302 (96.15%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112876365-A | Methyl rupestonic acid derivative containing cinnamoyl and preparation method and application thereof | 20210220 |
CN-112209930-A | Istradefylline derivative and preparation method and application thereof | 20201023 |
CN-111892537-A | Aporphine alkaloid derivative and preparation method and application thereof | 20200804 |
WO-2021193349-A1 | Hydrophilic oil repellent polymer | 20200324 |
CN-111358801-A | Application of tenuifolin F in preparing medicine for preventing and treating Huntington disease | 20200321 |
PMID | Publication Date | Title | Journal |
29940154 | 20180801 | Methyl ferulic acid attenuates ethanol-induced hepatic steatosis by regulating AMPK and FoxO1 Pathways in Rats and L-02 cells | Chemico-biological interactions |
23571415 | 20130601 | Structure-based identification of OATP1B1/3 inhibitors | Molecular pharmacology |
22925447 | 20120915 | Structure-anti-leukemic activity relationship study of ortho-dihydroxycoumarins in U-937 cells: key role of the δ-lactone ring in determining differentiation-inducing potency and selective pro-apoptotic action | Bioorganic & medicinal chemistry |
22865606 | 20120901 | Absorption of dimethoxycinnamic acid derivatives in vitro and pharmacokinetic profile in human plasma following coffee consumption | Molecular nutrition & food research |
23055639 | 20120701 | Trianthema portulacastrum Linn. (Bishkhapra) | Pharmacognosy reviews |
Complexity: | 237 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 1 |
Exact Mass: | 208.07355886 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 208.07355886 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 55.8 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.8 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS