missing translation for 'onlineSavingsMsg'
Learn More
Please login to your online account to display your discounted pricing

4-Bromo-4'-hydroxybiphenyl, 98%, Thermo Scientific Chemicals

Supplier:  Thermo Scientific Chemicals A1081922

 View more versions of this product

Catalog No. AAA1081922



Description

Description

A biphenyl starting material. 4-Bromo-(1,1-biphenyl)-4-ol is a useful intermediate. Vinylation of 4-bromo-4-hydroxybiphenyl and ethyl acrylate using Pd (OAc) 2/PPh 3 catalyst was studied. Ethyl 4-(4-hydroxyphenyl) cinnamate was formed as the vinylation product, while, 4-hydroxybiphenyl and ethyl cinnamate were formed as side products. Preparation of 4-cyano-4'-hydroxybiphenyl This was prepared from 4-bromo-4'-benzenesulphonyloxybiphenyl by first hydrolysing it to 4-bromo-4-hydroxybiphenyl using sodium hydroxide dissolved in a mixture of water and dioxan. The syntheses of the Nanocomposite dendrimers based on cyclic phosphazene cores: Amorphous materials, were accomplished by following a modified literature procedure by reacting phosphonitrilic chloride trimer with 4-bromophenol or 4-bromo-4-hydroxybiphenyl, respectively, in the presence of K 2 CO 3 in tetrahydrofuran (THF).

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
A biphenyl starting material. 4′-Bromo-(1,1′-biphenyl)-4-ol is a useful intermediate. Vinylation of 4-bromo-4′-hydroxybiphenyl and ethyl acrylate using Pd (OAc) 2/PPh 3 catalyst was studied. Ethyl 4-(4′-hydroxyphenyl) cinnamate was formed as the vinylation product, while, 4-hydroxybiphenyl and ethyl cinnamate were formed as side products. Preparation of 4-cyano-4′-hydroxybiphenyl This was prepared from 4-bromo-4′-benzenesulphonyloxybiphenyl by first hydrolysing it to 4-bromo-4-hydroxybiphenyl using sodium hydroxide dissolved in a mixture of water and dioxan. The syntheses of the Nanocomposite dendrimers based on cyclic phosphazene cores: Amorphous materials, were accomplished by following a modified literature procedure by reacting phosphonitrilic chloride trimer with 4-bromophenol or 4-bromo-4′-hydroxybiphenyl, respectively, in the presence of K 2 CO 3 in tetrahydrofuran (THF).

Solubility
Soluble in water (partly), and methanol.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
Specifications

Specifications

4-Bromo-4'-hydroxybiphenyl
163°C to 168°C
MFCD00059076
4-bromo-4'-hydroxybiphenyl, 4'-bromo-1,1'-biphenyl-4-ol, 4-4-bromophenyl phenol, 4'-bromobiphenyl-4-ol, 4-hydroxy-4'-bromobiphenyl, 1,1'-biphenyl-4-ol, 4'-bromo, 4-bromo-4-hydroxybiphenyl, pubchem23025
ARUBXNBYMCVENE-UHFFFAOYSA-N
4-(4-bromophenyl)phenol
95093
98%
29558-77-8
C12H9BrO
100 g
Soluble in water (partly),and methanol.
C1=CC(=CC=C1C2=CC=C(C=C2)Br)O
249.107
249.11

Chemical Identifiers

29558-77-8
249.107
ARUBXNBYMCVENE-UHFFFAOYSA-N
95093
C1=CC(=CC=C1C2=CC=C(C=C2)Br)O
C12H9BrO
MFCD00059076
4-bromo-4'-hydroxybiphenyl, 4'-bromo-1,1'-biphenyl-4-ol, 4-4-bromophenyl phenol, 4'-bromobiphenyl-4-ol, 4-hydroxy-4'-bromobiphenyl, 1,1'-biphenyl-4-ol, 4'-bromo, 4-bromo-4-hydroxybiphenyl, pubchem23025
4-(4-bromophenyl)phenol
Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

TSCA : No

Recommended Storage : Ambient temperatures

SDS
Documents

Documents

Promotions

Promotions

RUO – Research Use Only