Basic information Safety Supplier Related

1,2-Dihydrobenzocyclobutene-1-carboxylic acid methyl ester

Basic information Safety Supplier Related

1,2-Dihydrobenzocyclobutene-1-carboxylic acid methyl ester Basic information

Product Name:
1,2-Dihydrobenzocyclobutene-1-carboxylic acid methyl ester
Synonyms:
  • 1,2-Dihydrobenzocyclobutene-1-carboxylic acid methyl ester
  • Bicyclo[4.2.0]octa-1,3,5-triene-7-carboxylic acid methyl ester
  • Benzocyclobutene-1-carboxylic acid methyl ester
  • Methyl bicyclo[4.2.0]octa-1,3,5,7-tetraene-7-carboxylate
  • Methyl bicyclo[4.2.0]octa-1,3,5-triene-7-carboxylate
  • Methyl bicyclo[4.2.0]octa-1,3
CAS:
35095-07-9
MF:
C10H10O2
MW:
162.19
EINECS:
233-305-4
Product Categories:
  • Aluminium foil bag/Fluoride bottle or on your request
Mol File:
35095-07-9.mol
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1,2-Dihydrobenzocyclobutene-1-carboxylic acid methyl ester Chemical Properties

Boiling point:
68℃ (25 Torr)
Density 
1.171±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
InChI
InChI=1S/C10H10O2/c1-12-10(11)9-6-7-4-2-3-5-8(7)9/h2-5,9H,6H2,1H3
InChIKey
XWGYSWFRKUQSLL-UHFFFAOYSA-N
SMILES
C12C(C(C(OC)=O)C1)=CC=CC=2
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1,2-Dihydrobenzocyclobutene-1-carboxylic acid methyl ester Usage And Synthesis

Synthesis

88284-48-4

292638-85-8

35095-07-9

GENERAL METHOD: A mixture of 2-(trimethylmethylsilyl)phenyl trifluoromethanesulfonate (3 mmol, 2.0 eq.), compound (CAS:292638-85-8, 1.0 eq.) and anhydrous cesium fluoride (6.0 eq.) was dissolved in dry acetonitrile (15 mL). The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, 20 mL of water was added to the mixture and extracted with dichloromethane (3 x 20 mL). The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: petroleum ether) to afford the target product methyl benzocyclobutene-1-carboxylate (3c-6c). Compound 5c: pale yellow oil.1H NMR (400 MHz, CDCl3): δ 7.26-7.24 (m, 2H), 7.18 (d, 1H, J = 4 Hz), 7.11 (d, 1H, J = 4 Hz), 4.32 (t, 1H, J = 4 Hz), 3.73 (d, 3H, J = 8 Hz), 3.48 (d, 2H, J = 4 Hz). These data are in good agreement with literature values [14].

References

[1] Chinese Chemical Letters, 2014, vol. 25, # 12, p. 1535 - 1539

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