Home Cart Sign in  
Chemical Structure| 7345-76-8 Chemical Structure| 7345-76-8

Structure of 7345-76-8

Chemical Structure| 7345-76-8

*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 [ 7345-76-8 ]

CAS No. :7345-76-8
Formula : C12H10O4S
M.W : 250.27
SMILES Code : O=C(C1=CC2=CC(C(OC)=O)=CC=C2S1)OC

Safety of [ 7345-76-8 ]

Application In Synthesis of [ 7345-76-8 ]

* 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 [ 7345-76-8 ]

[ 7345-76-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2365-48-2 ]
  • [ 148625-35-8 ]
  • [ 7345-76-8 ]
YieldReaction ConditionsOperation in experiment
323 mg With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 3h; 12223] A mixture of 1.00 g of methyl 3-formyl-4-nitroben- zoate, 609 mg of methyl thioglycolate, 761 mg of potassium carbonate, and 15 ml of N,N-dimethylformamide was stirred for 3 hours at 60° C. The reaction mixture was cooled to room temperature, water was added to the reaction mixture, and extraction was performed three times with ethyl acetate. The collected organic layer was washed with water and saturated saline, dried over magnesium sulfate, and then concentrated under reduced pressure. The residues were subjected to silica gel colunm chromatography, thereby obtaining 323 mg of dimethyl benzo[b]thiophene-2,5-dicarboxylate (hereinafter, described as a ?compound 58 of the present invention?).12224] Compound 58 of the Present Invention12225] ?H-NMR (CDC13) oe: 8.60-8.56 (m, 1H), 8.13-8.10 (m, 2H), 7.93-7.91 (m, 1H), 3.97 (s, 3H), 3.97 (s, 3H)
323 mg With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 3h; A mixture of 1.00 g of <strong>[148625-35-8]methyl 3-formyl-4-nitrobenzoate</strong>, 609 mg of methyl thioglycolate, 761 mg of potassiumcarbonate, and 15 ml of N,N-dimethylformamide was stirred for 3 hours at 60°C. The reaction mixture was cooled toroom temperature, water was added to the reaction mixture, and extraction was performed three times with ethyl acetate.The collected organic layer was washed with water and saturated saline, dried over magnesium sulfate, and thenconcentrated under reduced pressure. The residues were subjected to silica gel column chromatography, thereby obtaining323 mg of dimethyl benzo[b]thiophene-2,5-dicarboxylate.
 

Historical Records

Technical Information

Categories