Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 877-53-2 Chemical Structure| 877-53-2

Structure of 877-53-2

Chemical Structure| 877-53-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

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

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

Alternative Products

Product Details of [ 877-53-2 ]

CAS No. :877-53-2
Formula : C10H12O2
M.W : 164.20
SMILES Code : CC(OC1=CC=C(C)C=C1C)=O
English Name :2,4-Dimethylphenyl acetate

Safety of [ 877-53-2 ]

Application In Synthesis of [ 877-53-2 ]

* 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 [ 877-53-2 ]

[ 877-53-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 452-65-3 ]
  • [ 415974-43-5 ]
  • [ 877-53-2 ]
YieldReaction ConditionsOperation in experiment
78% With iron sulfide; boron trifluoride In dimethyl sulfoxide at 20℃; for 48h; Inert atmosphere; Irradiation; 15 Example 15: Preparation of 2,4-Dimethylphenylacetic acid A suitable magnetic ball was added to a 10 mL quartz reaction tube, followed by 0.3 mmol of 2,4-dimethylfluorobenzene, 0.03 mmol of iron catalyst FeS, 0.6 mmol of BF3, and 0.9 mmol of CH3COOAg, and 3 mL of dimethyl sulfoxide solvent. A T-connector was inserted into the reaction tube, a balloon was attached, and the reaction mixture was frozen with liquid nitrogen. The gas in the reaction tube and balloon was evacuated using an oil pump, and nitrogen was introduced. After thawing, the reaction was stirred at room temperature under blue light (455 nm, 50 W) for 48 h, and the reaction was monitored by thin-layer chromatography. Finally, column chromatography was used to separate the final product, 2,4-dimethylphenylacetic acid, in 78.0% yield.
  • 2
  • [ 452-65-3 ]
  • [ CAS Unavailable ]
  • [ 877-53-2 ]
YieldReaction ConditionsOperation in experiment
79% With iron sulfide; boron trifluoride In dimethyl sulfoxide at 20℃; for 48h; Inert atmosphere; Irradiation; 14 Example 14, Preparation of 2,4-Dimethylphenylacetic Acid Ester. A suitable magnetic ball was added to a 10 mL quartz reaction tube, followed by 0.3 mmol of 2,4-dimethylfluorobenzene, 0.03 mmol of iron metal catalyst FeS, 0.6 mmol of BF3, 0.9 mmol of CH3COOK, and 3 mL of dimethyl sulfoxide solvent. A T-connector was inserted into the reaction tube, a balloon was attached, and the reaction mixture was frozen with liquid nitrogen. The gas in the reaction tube and balloon was evacuated using an oil pump, and nitrogen was introduced. After thawing, the reaction was stirred at room temperature for 48 h under blue light (455 nm, 50 W), and the reaction was monitored by thin-layer chromatography. Finally, column chromatography was used to separate the final product, 2,4-dimethylphenylacetic acid ester, with a yield of 79.0%.
 

Historical Records