Home Cart Sign in  
Chemical Structure| 116406-19-0 Chemical Structure| 116406-19-0

Structure of 116406-19-0

Chemical Structure| 116406-19-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 116406-19-0 ]

CAS No. :116406-19-0
Formula : C12H14O5
M.W : 238.24
SMILES Code : O=C(O)/C=C/C1=CC=C(OC)C(OC)=C1OC
MDL No. :MFCD00014376

Safety of [ 116406-19-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P280-P304+P340-P305+P351+P338-P405-P501

Application In Synthesis of [ 116406-19-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 116406-19-0 ]

[ 116406-19-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 116406-19-0 ]
  • [ 33130-04-0 ]
YieldReaction ConditionsOperation in experiment
100% With palladium 10% on activated carbon; hydrogen; In ethanol; ethyl acetate; for 18h; Step 2 Synthesis of 3-(2,3,4-trimethoxyphenyl)propanoic acid 1.3 To a stirred solution of (E)-3-(2,3,4-trimethoxyphenyl)acrylic acid 1.2 (500 mg, 2.11 mmol) in a 1:1 mixture of ethanol and ethyl acetate (10 mL) was added at catalytic amount of 10% Pd/C under an atmosphere of hydrogen gas (balloon). After 18 h the reaction mixture was filtered and the solvent was removed in vacuo to afford an off-white solid. The resulting residue redissolved in diethyl ether (20 mL) and was washed with 2.5M aq. NaOH (3*20 mL). The combined aqueous extracts were acidified with 2M aq. HCl and the product was extracted with diethyl ether (3*30 mL). The combined ether extracts were dried over MgSO4, filtered and concentrated in vacuo to afford 3-(2,3,4-trimethoxyphenyl)propanoic acid 1.3 as a white solid (500 mg, 100%). 1H NMR (CDCl3, 400 MHz) δH ppm: 2.66 (2H, t, J=7.5 Hz, CH2), 2.90 (2H, t, J=7.5 Hz, CH2), 3.86 (3H, s, OMe), 3.88 (3H, s, OMe), 3.92 (3H, s, OMe), 6.61 (1H, d, J=8.0 Hz, ArH), 6.87 (1H, d, J=8.0 Hz, ArH) 13C NMR (CDCl3, 400 MHz) δc ppm: 24.72 (CH2), 34.45 (CH2), 55.53 (OMe), 60.27 (OMe), 60.41 (OMe), 106.62 (ArCH), 123.33 (ArCH), 125.60 (ArC), 141.74 (ArC), 151.44 (ArC), 152.06 (ArC), 191.57 (C=O) νmax (KBr)/cm-1 3004.2, 2834.9, 1712.9, 1599.5 HRMS: calculated 263.0895, found 263.0845, molecular formula (C12H16O5Na).; Melting point: 65-67 C.
98% With hydrogen;palladium 10% on activated carbon; In methanol; for 24h; 27. 3-(2',3',4'-Trimethoxyphenyl)propanoic acid (27); Through a suspension of 10% Pd/C (396 mg) and cinnamic acid 25 (4.82 g, 20.19 mmol) in MeOH (100 mL), H2 gas (in balloons) was passed for 24 h. The reaction was monitored for completion by filtering a little amount of the reaction mixture through CELITE (diatomaceous earth) and evaporating the solvent to record NMR data. On completion, the reaction mixture was filtered through CELITE (diatomaceous earth) and the solvent was evaporated under reduced pressure to obtain propanoic acid analog 27 (4.73 g, 19.68 mmol, 98% yield), as a liquid.1H NMR (500 MHz, CDCl3) δ 6.85 (1H, d, J=8.5 Hz, H-6), 6.59 (1H, d, J=8.5 Hz, H-5), 3.90 (3H, s, OCH3-2'), 3.86 (3H, s, OCH3-3'), 3.84 (3H, s, OCH3-4'), 2.89 (2H, t, J=7.5, 8.0 Hz, H-3), 2.64 (2H, s, t, J=7.5, 8.0 Hz, H-2). 13C NMR (126 MHz, CDCl3) δ 179.4 (C, C-1), 152.5 (C, C-4'), 151.9 (C, C-2'), 142.2 (C, C-3'), 126.1 (C, C-1'), 123.8 (CH, C-6'), 107.1 (CH, C-5'), 60.8 (CH3, OCH3-2'), 60.7 (CH3, OCH3-3'), 56.0 (CH3, OCH3-4'), 34.9 (CH2, C-2), 25.2 (CH2, C-3).
 

Historical Records