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7073-69-0

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7073-69-0 Usage

General Description

2-(2-Bromophenyl)-2-propanol, also known as α-bromo-α-(2-hydroxy-2-phenylethyl)benzyl alcohol, is an organic compound with the molecular formula C9H11BrO. It is a white solid with a faint, pleasant odor and is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is a chiral molecule, meaning it has two enantiomers that are mirror images of each other. 2-(2-Bromophenyl)-2-propanol has a wide range of applications in the pharmaceutical and chemical industries, including as a reagent in the production of various drugs and as a chiral building block for the synthesis of complex organic molecules. Overall, 2-(2-Bromophenyl)-2-propanol plays a crucial role in the development of various pharmaceutical and chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 7073-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7073-69:
(6*7)+(5*0)+(4*7)+(3*3)+(2*6)+(1*9)=100
100 % 10 = 0
So 7073-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11BrO/c1-9(2,11)7-5-3-4-6-8(7)10/h3-6,11H,1-2H3

7073-69-0SDS

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 2-(2-bromophenyl)propan-2-ol

1.2 Other means of identification

Product number -
Other names o-bromo-1-methyl-1-phenylethanol

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:7073-69-0 SDS

7073-69-0Relevant articles and documents

Synthesis method of montelukast sodium intermediate

-

Paragraph 0067; 0068, (2021/03/03)

The invention is applicable to the technical field of medicine synthesis, and provides a synthesis method of a montelukast sodium intermediate. The method comprises the following steps of: generatinga compound II from halogenated benzene under the action

BORON CONTAINING COMPOUNDS AND THEIR USES

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Paragraph 0224-0225, (2020/03/29)

The present disclosure contemplates novel boron-containing compounds and their uses as active agents that exhibit pesticidal activity such as antimicrobial, insecticidal, arachnicidal, and/or anti parasitic activity. An agrochemical composition containing such a compound and its use in, animal health, agriculture, or horticulture is also contemplated. A method for promoting plant performance and/or controlling, reducing, preventing, ameliorating, or inhibiting microbes, insects, arachnids, and/or parasites on or in an animal, a plant, a plant part, plant propagation material, and/or harvested fruits or vegetables is also contemplated.

Rh-Catalyzed Asymmetric Hydrogenation of α,β- and β,β-Disubstituted Unsaturated Boronate Esters

Hou, Guohua,Shen, Xin,Yan, Qiaozhi,Zi, Guofu

, (2020/05/08)

A highly enantioselective hydrogenation of α,β-unsaturated boronate esters catalyzed by Rh-(S)-DTBM-Segphos complex has been developed. Both (Z)-α,β- and β,β-disubstituted substrates can be successfully hydrogenated to afford chiral boronates with excellent enantioselectivities, up to 98 % ee. Furthermore, the obtained chiral boronate esters, as important versatile synthetic intermediates are successfully transformed to the corresponding chiral alcohols, amines and other important derivatives with maintained enantioselectivities.

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