Basic information Safety Supplier Related

1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID

Basic information Safety Supplier Related

1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID Basic information

Product Name:
1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID
Synonyms:
  • 1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID
  • 1-(4-BroMophenyl)-1-cyclopropanecarboxylic acid
  • Cyclopropanecarboxylic acid, 1-(4-broMophenyl)-
  • 1-(4-broMophenyl)cyclopropane-1-carboxylic acid
  • EOS-60374
  • 345965-52-8, MFCD07374439
  • CAS:345965-52-8
CAS:
345965-52-8
MF:
C10H9BrO2
MW:
241.08
Product Categories:
  • pharmacetical
  • Carboxylic Acids
  • Carboxylic Acids
  • Ring Systems
Mol File:
345965-52-8.mol
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1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID Chemical Properties

Melting point:
160-165°
Boiling point:
354.3±35.0 °C(Predicted)
Density 
1.670±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
4.14±0.20(Predicted)
Appearance
White to light yellow Solid
InChI
InChI=1S/C10H9BrO2/c11-8-3-1-7(2-4-8)10(5-6-10)9(12)13/h1-4H,5-6H2,(H,12,13)
InChIKey
BYJIXWOWTNEVFO-UHFFFAOYSA-N
SMILES
C1(C2=CC=C(Br)C=C2)(C(O)=O)CC1
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Safety Information

HS Code 
2917399590
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1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID Usage And Synthesis

Synthesis

124276-67-1

345965-52-8

General procedure for the synthesis of 1-(4-bromophenyl)cyclopropanecarboxylic acid from 1-(4-bromophenyl)cyclopropanecarbonitrile: A mixture of 1-(4-bromophenyl)cyclopropanecarbonitrile (7.5 g, 33.78 mmol), potassium hydroxide (7.6 g, 135 mmol), and ethylene glycol (50 mL) was heated to 160 °C for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature, water (200 mL) was added and the pH was adjusted to 3~4 with dilute hydrochloric acid to acidify the reaction mixture. Subsequently, the product was precipitated with 2N hydrochloric acid. The precipitate was collected by filtration to afford 1-(4-bromophenyl)cyclopropanecarboxylic acid (5.6 g, 69% yield). Mass spectrum (ESI) m/z (M+H)+ 240.

References

[1] Patent: US6359135, 2002, B1. Location in patent: Page column 113
[2] Patent: US6369225, 2002, B1. Location in patent: Page column 42, 112
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 16, p. 6003 - 6017
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 3, p. 887 - 892
[5] Patent: WO2013/25733, 2013, A1. Location in patent: Paragraph 0490

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