Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 57965-29-4 Chemical Structure| 57965-29-4

Structure of 57965-29-4

Chemical Structure| 57965-29-4

*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 [ 57965-29-4 ]

CAS No. :57965-29-4
Formula : C3H5FO2
M.W : 92.07
SMILES Code : C[C@@H](C(O)=O)F
MDL No. :MFCD18974368
InChI Key :ZVZPFTCEXIGSHM-REOHCLBHSA-N
Pubchem ID :11040627

Safety of [ 57965-29-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H227-H302-H314-H319
Precautionary Statements:P210-P264-P270-P280-P301+P312+P330-P301+P330+P331-P303+P361+P353-P304+P340+P310-P305+P351+P338-P337+P313-P363-P370+P378-P403+P235-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 57965-29-4 ]

* 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 [ 57965-29-4 ]

[ 57965-29-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 57965-29-4 ]
  • [ 430-99-9 ]
  • 2
  • [ 349-43-9 ]
  • [ 57965-29-4 ]
YieldReaction ConditionsOperation in experiment
78.3% With sulfuric acid; In water; at 120℃; for 1h; Preparation 362 2-fluoropropionic acid Heat a solution of <strong>[349-43-9]ethyl 2-fluoropropionate</strong> (0.30 g, 2.50 mmol) in 5M sulfuric acid (5 mL) at 120° C. for 1 hour. Saturate the solution with sodium chloride and extract with diethyl ether (4*40 mL). Dry the combined organic extracts with magnesium sulfate and concentrate under reduced pressure to provide 0.18 g (78.3percent) of the title compound. GCMS: m/z=92.0 [M]
With sodium hydroxide; In tetrahydrofuran; for 2h; 4.2.6.1 2-Fluoropropanoic acid A total of 6.6 mL (11.0 mmol) of a 1.0 g/20 mL NaOH solution was added to a solution of 1.0 mL (10.0 mmol) of <strong>[349-43-9]ethyl 2-fluoropropanoate</strong> in tetrahydrofuran (THF), and the mixture was reacted under backstreaming for 2 h. After the solution reached room temperature, the pH was adjusted to 6.0, and dichloromethane was added until a total volume of 100 mL was achieved.
  • 3
  • [ 57965-29-4 ]
  • [ 120-35-4 ]
  • [ 1400659-65-5 ]
YieldReaction ConditionsOperation in experiment
67% With benzotriazol-1-ol; diisopropyl-carbodiimide; In tetrahydrofuran; dichloromethane; at 20℃; for 0.5h; 4.2.6.2 3-(2-Fluoropropanamido)-4-methoxy-N-phenylbenzamide (1m) A total of 0.17 mL (0.18 mmol) of DIC and 0.24 g (0.18 mmol) of HOBt were added to a dichloromethane solution of 14.0 mL (0.12 mmol) of 2-fluoropropanoic acid and THF at room temperature, which was stirred for 0.5 h. Then, 0.35 g (0.14 mmol) of 1-M5 was added to the mixture, and after approximately 3 h, 0.5 N NaOH was added to the solution. The lower layer was isolated, and 0.5 N HCl was added until the aqueous solution was neutral. The dichloromethane layer was washed three times with 10 mL of water, and MgSO4 was then added. After 2 h, the solution was filtered, and the solvent was removed. The residue was purified by column chromatography on silica gel (eluent: petroleum ether:ethyl acetate = 4:1) to yield the desired compound as a white solid (yield: 67%, HPLC purity: 99.40%). Mp: 182-184 C. 1H NMR (400 MHz, DMSO-d6) delta (ppm): 10.12 (1H, s, NH), 9.22 (1H, s, NH), 8.49 (1H, s, PhH), 7.81 (1H, d, J = 6.0 Hz, PhH), 7.78 (2H,d, J = 7.6 Hz, PhH), 7.33 (2H, t, J = 7.6 Hz, PhH), 7.20 (1H, d, J = 8.8 Hz, PhH), 7.07 (1H, m, PhH), 5.34 (1H, qq, JH-H = 6.4 Hz, JH-F = 48.8 Hz, CH), 3.93 (3H, s, OCH3), 1.55 (3H, dd, JH-H = 6.4 Hz, JH-F = 20.8 Hz, CH3). HRMS-ESI (m/z): calculated for C17H17N2O3F (M)+: 316.11803; measured: 316.12177.
 

Historical Records

Technical Information

Categories