2316-62-3

Basic information

• Product Name: 3,5-DIBROMO-4-HYDROXYBENZYL ALCOHOL
• Synonyms: 3,5-DIBROMO-4-HYDROXYBENZYL ALCOHOL;RARECHEM AL BD 0231;2,6-Dibromo-4-(hydroxymethyl)phenol
• CAS NO: 2316-62-3
• Molecular Formula: C₇H₆Br₂O₂
• Molecular Weight: 281.93
• Product Categories: Benzhydrols, Benzyl & Special Alcohols
• Mol File: 2316-62-3.mol
• Article Data: 2

Chemical Properties

• Melting Point: 117 °C
• Boiling Point: 324.7±37.0 °C(Predicted)
• Appearance: /
• Density: 2.103±0.06 g/cm3(Predicted)
• PKA: 6.69±0.23(Predicted)
• CAS DataBase Reference: 3,5-DIBROMO-4-HYDROXYBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIBROMO-4-HYDROXYBENZYL ALCOHOL(2316-62-3)
• EPA Substance Registry System: 3,5-DIBROMO-4-HYDROXYBENZYL ALCOHOL(2316-62-3)

Safety Data

• Hazardous Substances Data: 2316-62-3(Hazardous Substances Data)

Upstream product

• 5532-75-2 2,6-dibromo-4-bromomethyl-phenol 
• 67-64-1 acetone 
• 2973-77-5 3,5-dibromo-4-hydroxybenzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 2432-14-6 3,5-dibromo-4-hydroxytoluene 

Downstream Products

• 99586-33-1 2,6-dibromo-2',6'-dichloro-4,4'-methanediyl-di-phenol 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 20244-61-5 2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one 
• 19643-45-9 2,6-dibromo-1,4-benzoquinone 
• 1089665-95-1 tert-butyldimethylsilyl 2,6-dibromo-4-(tert-butyldimethylsilyloxymethyl)pheny ether 
• 52193-43-8 thelephenol 
• 2467-03-0 2-[(4-hydroxyphenyl)methyl]phenol 
• 2973-77-5 3,5-dibromo-4-hydroxybenzaldehyde 
• 52193-44-9 2,4'-Dihydroxy-5-formyl-3,3',5'-tribromdiphenylmethan 
• 91805-66-2 2',6'-dibromo-4-chloro-2,4'-methanediyl-di-phenol 
• 71119-02-3 3,5-dibromo-4-hydroxy benzyl alcohol methyl ether 
• 74849-03-9 2-acetoxy-5-acetoxymethyl-1,3-dibromo-benzene 
• 1059183-82-2 1,3-dibromo-5-hydroxymethyl-2-octadecyloxybenzene 
• 1059183-81-1 1,3-dibromo-5-hydroxymethyl-2-dodecyloxybenzene 

Relevant articles and documents

Synthesis of biaryl compounds through three-component assembly: Ambidentate effect of the tert-butyldimethylsilyl group for regioselective diels-alder and hiyama coupling reactions

Two for the price of one: A method has been developed for the regiocontrolled synthesis of multisubstituted biaryl derivatives. This protocol involves the use of the tert-butyldimethylsilyl (TBDMS) group to direct the regioselective Diels-Alder reaction of a 3-TBDMS-benzyne with a furan derivative and a subsequent Hiyama cross-coupling reaction of the TBDMS group with aryl iodides (see scheme).