Product
Supplier
Encyclopedia
Inquiry
Home > Encyclopedia > 1,3-DIBROMO-4-IODOBENZENE

1,3-DIBROMO-4-IODOBENZENE

1,3-DIBROMO-4-IODOBENZENE structure

1,3-DIBROMO-4-IODOBENZENE 

structure
  • CAS No:

    19393-94-3

  • Formula:

    C6H3Br2I

  • Chemical Name:

    1,3-DIBROMO-4-IODOBENZENE

  • Synonyms:

    2,4-dibromo-1-iodobenzene;2,4-Dibromoiodobenzene;1,3-Dibromo-4-iodobenzene;Benzene, 2,4-dibromo-1-iodo-;2,4-dibromo-1-iodo-benzene;2,4-dibromoiodobenzene;;1-Jodo-2,4-dibromobenzol;1-Iodo-2,4-dibromobenzene;1,3-dibromo-4-iodobenzene;;1-iodo-2,4-dibromobenzene;

  • Categories:

    Organic Chemistry  >  Heterocyclic Ring

1,3-DIBROMO-4-IODOBENZENE Basic Attributes

361.81

359.76500

DTXSID80541567

2903999090

Characteristics

0

4

2.514±0.06 g/cm3(Predicted)

45-46℃

299.1±20.0 °C(Predicted)

134.7ºC

1.682

0.00217mmHg at 25°C

1,3-DIBROMO-4-IODOBENZENE Use and Manufacturing

[Production Example 1]; The following Indenopyrene Compound A was produced through the following synthesis route.; Synthesis of Intermediate A1; 2, 4-Dibromoaniline (10 g, 40 mmoles) was suspended in hydrochloric acid water (40 mL of concentrated hydrochloric acid and 30 mL of water), and the suspension was cooled on an ice/salt bath at -8°C. A sodium nitrite aqueous solution (3.0 g, 43 mmoles, 1.1 eq. /15 mL) was gradually added dropwise thereto over 10 minutes, and the mixture was stirred at from -10°C to 0°C for 30 minutes, thereby preparing a diazonium salt. The reaction solution was gradually added dropwise to a potassium iodide aqueous solution (60 g, 0.36 moles, 9 eq. /180 mL) at room temperature over 20 minutes. The reaction mixture was stirred at room temperature for 3 hours, to which was then added dichloromethane (200 mL), and subsequently, sodium hydrogensulfite (2 g) was added, thereby deactivating generated iodine. An organic layer was aliquoted, washed with a sodium hydrogensulfite aqueous solution (100 mL) and saturated salt water (30 mL) and then dried over anhydrous magnesium sulfate, and the solvent was then distilled off to obtain a red liquid. This was purified by means of column chromatography (silica gel/hexane) to obtain a white solid (11.0 g, 76percent).

Computed Properties

Molecular Weight:361.80
XLogP3:4
Exact Mass:361.76257
Monoisotopic Mass:359.76462
Heavy Atom Count:9
Complexity:97.1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Recommended Suppliers of 1,3-DIBROMO-4-IODOBENZENE

Scan the QR Code to Share

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.