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3',3'',5',5''-TETRABROMOPHENOLPHTHALEIN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76-62-0

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76-62-0 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 76-62-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76-62:
(4*7)+(3*6)+(2*6)+(1*2)=60
60 % 10 = 0
So 76-62-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H10Br4O4/c21-13-5-9(6-14(22)17(13)25)20(10-7-15(23)18(26)16(24)8-10)12-4-2-1-3-11(12)19(27)28-20/h1-8,25-26H

76-62-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3',3'',5',5''-Tetrabromophenolphthalein

1.2 Other means of identification

Product number -
Other names 3',3'',5',5''-TETRABROMOPHENOLPHTHALEIN

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76-62-0 SDS

76-62-0Relevant academic research and scientific papers

COMPLEX FORMATION OF CYCLOMALTO-OCTAOSE WITH TETRABROMOPHENOLPHTHALEIN AND SOME RELATED COMPOUNDS

Barcza, Lajos,Buvari-Barcza, Agnes

, p. 103 - 110 (1989)

The interactions of cyclomalto-octaose (γ-cyclodextrin) with some phthalein-type acid-base indicators have been investigated photometrically.Bromine substituents enhance the formation of complexes and tetrabromophenolphthalein forms the most stable complex (K 6.0 x 1E3).This stability and other phenomena suggest that the host and guest are involved in a three-site interaction.

Crystal structure and catalytic properties of a vanadium complex cis-[VO2(Him-py)(im-py)]2·3H2O

Sun, Meng,Zhang, Shaowei,Zhang, Jie,Xia, Wen,Chen, Jialiang,Yu, Xianyong

, p. 1899 - 1909 (2019/06/04)

The coordination behavior of Him-py (2-(1H-imidazol-2-yl)pyridine) toward vanadium has been explored. The six-coordinate complex, cis-[VO2(Him-py)(im-py)]2·3H2O (1), was synthesized by the coordination reaction of NH4VO3 and Him-py in the aqueous methanol solution, which was characterized by single-crystal X-ray technology. It belongs to the monoclinic space group P21/n with a = 8.0756(6), b = 19.3531(15), c = 11.4433(8), β = 106.905(2), V = 1711.2(2), and Z = 2. The crystal structure shows that the six-coordinate vanadium is bonded to two cis-oxido ligands and two bidentate ligands, Him-py and im-py. Interestingly, when crystals of 1 were immersed in H2O2, a peroxovanadium compound, (H2im-py)[OV(O2)2(Him-py)] (2), was obtained, which crystallizes in the orthorhombic space group Fdd2 with a = 22.600(2), b = 22.7259(13), c = 18.0146(11), V = 9252.4(12), and Z = 16, and consists of a seven-coordinate peroxovanadate(V) ion, one Him-py and one H2im-py ligand. Moreover, we also studied the catalytic activity of 1 in the oxidative bromination of phenol/aniline-like compounds towards mimicking bromoperoxidase reactivity.

1-Benzyl-4-aza-1-azoniabicyclo[2.2.2]octane tribromide as a regenerable and useful reagent for bromination of phenols under mild conditions

Hajipour, Abdol R.,Pourmousavi, Seied A.,Ruoho, Arnold E.

, p. 796 - 800 (2007/10/03)

1-Benzyl-4-aza-1-azoniabicyclo[2.2.2]octane tribromide has been examined over several phenolic compounds under mild conditions. The reaction gives brominated phenols in good to excellent yields. Straightforward work-up of the reaction yields pure products in several cases.

A controlled and selective bromination of phenols by benzyltriphenylphosphonium tribromide

Hajipour, Abdol Reza,Mallakpour, Shadpour E.,Imanieh, Hossein,Pourmousavi, Seied A.

, p. 272 - 275 (2007/10/03)

Reactions of phenols with benzyltriphenylphosphonium tribromide in dichloromethane-methanol mixture (2:1) gave mono, di and tri brominated phenols at room temperature with high selectivity and good yields.

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