1,3-DIBROMO-4-IODOBENZENE
-
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:
-
CAS No:
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
-
CN
5 YRS
Business licensedTrader Supplier of Intermediates,Building blocks,API,Silicones,Peptides,Lab chemicals,Biochemicals,Pharmaceuticals,Screening Compounds,Food Additives -
CN
5 YRS
Business licensedTrader Supplier of PVC resin,pvc paste resin,melamine
Learn More Other Chemicals
-
INCANINE
480-77-3
-
Tricyclene
508-32-7
-
Ethanol, 2,2′-oxybis-, polymer with 2-(chloromethyl)oxirane
25928-94-3
-
Z-Phe-Arg-AMC Formula
65147-22-0
-
METHYL5-BROMO-2-IODOBENZOATE Formula
181765-86-6
-
5β-Cholestane Formula
481-20-9
-
4,5-Dimethyl-2(3H)-thiazolethione Structure
5351-51-9
-
Cinchonamine Structure
482-28-0
-
What is C.I. Basic Blue 15
4692-38-0
-
What is 1,4-Dioxa-8-azaspiro[4.5]decane
177-11-7