METHYL 2-(2-BROMOPHENYL)ACETATE

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Products Intro: Product Name:Methyl 2-(2-bromophenyl)acetate
CAS:57486-69-8
Purity:98%(Min.HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:57486-69-8
Purity:99% Package:25KG;5KG;1KG
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Purity:98% Package:5KG;1KG
Company Name: Wuhan Chemwish Technology Co., Ltd
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Products Intro: Product Name:Methyl2-(2-bromophenyl)acetate
CAS:57486-69-8
Purity:0.98 Package:1g;5g;25g;1699g

METHYL 2-(2-BROMOPHENYL)ACETATE manufacturers

METHYL 2-(2-BROMOPHENYL)ACETATE Basic information
Product Name:METHYL 2-(2-BROMOPHENYL)ACETATE
Synonyms:Methyl o-bromophenylacetate;2-broMobenzyl acetate;Methyl 2-(2-bromophenyl);(2-BROMO-PHENYL)-ACETIC ACID METHYL ESTER;Methyl 2-bromophenylacetate;METHYL 2-(2-BROMOPHENYL)ACETATE;Methyl 2-(2-bromophenyl)acetate 98%;Benzeneacetic acid,2-bromo-, methyl ester
CAS:57486-69-8
MF:C9H9BrO2
MW:229.07
EINECS:
Product Categories:Aromatic Building Blocks;blocks;Bromides;Carboxes
Mol File:57486-69-8.mol
METHYL 2-(2-BROMOPHENYL)ACETATE Structure
METHYL 2-(2-BROMOPHENYL)ACETATE Chemical Properties
Boiling point 264℃
density 1.445
Fp 114℃
storage temp. Keep in dark place,Inert atmosphere,2-8°C
form liquid
color Pale yellow
InChIInChI=1S/C9H9BrO2/c1-12-9(11)6-7-4-2-3-5-8(7)10/h2-5H,6H2,1H3
InChIKeyAMVCFIFDMKEIRE-UHFFFAOYSA-N
SMILESC1(CC(OC)=O)=CC=CC=C1Br
Safety Information
Hazard Codes Xi
Hazard Note Irritant/Keep Cold
HS Code 2916399090
MSDS Information
METHYL 2-(2-BROMOPHENYL)ACETATE Usage And Synthesis
UsesMethyl 2-(2-bromophenyl)acetate is a reagent in the synthesis of 2,3,3a,12b-Tetradehydro Asenapine (T291630). 2,3,3a,12b-Tetradehydro Asenapine is a degredation product of Asenapine (A788000), a combined serotonin (5HT2) and dopamine (D2) receptor antagonist; structurally related to Mianserin. Antipsychotic.
Synthesis
Methanol

67-56-1

2-Bromophenylacetic acid

18698-97-0

METHYL 2-(2-BROMOPHENYL)ACETATE

57486-69-8

General method: o-Bromophenylacetic acid (5.0 g, 18.18 mmol) was dissolved in methanol (50 mL) containing a catalytic amount of concentrated sulfuric acid and the reaction was refluxed for 30 minutes. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove the solvent. Water (30 mL) was added to the residue, which was subsequently extracted with dichloromethane (3 x 20 mL). The organic layers were combined, dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give the corresponding methyl 2-(2-bromophenyl)acetate products. The products were: methyl 2-(2-bromo-4,5-dimethoxyphenyl)acetate (S5a, 5.19 g, 99%, brown oil); methyl 2-(2-bromo-5-methoxyphenyl)acetate (S5b, 2.09 g, 99%, brown oil); methyl 2-(2-bromo-4-methoxyphenyl)acetate (S5c, 2.09 g, 99%, brown oil ); methyl 2-(2-bromophenyl)acetate (S5d, 5.27g, 99%, clear oil).

References[1] Journal of the American Chemical Society, 2003, vol. 125, # 11, p. 3268 - 3272
[2] Chemistry - An Asian Journal, 2011, vol. 6, # 8, p. 2040 - 2047
[3] Tetrahedron, 2013, vol. 69, # 42, p. 8914 - 8920
[4] Chemistry - A European Journal, 2016, vol. 22, # 34, p. 12166 - 12175
[5] Tetrahedron Letters, 2003, vol. 44, # 2, p. 331 - 334
Tag:METHYL 2-(2-BROMOPHENYL)ACETATE(57486-69-8) Related Product Information
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