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261711-20-0

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261711-20-0 Usage

General Description

1-(2-Bromo-4-fluorophenyl)ethanol is a chemical compound with the molecular formula C8H8BrFO. It is a colorless to pale yellow liquid that is typically used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its primary applications include being a building block in the production of various organic compounds, including but not limited to pharmaceuticals, dyes, and fragrances. It is important to handle and store this chemical with care, as it can be harmful if ingested, inhaled, or absorbed through the skin. Additionally, it should be kept away from sources of ignition and incompatible materials to prevent potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 261711-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,7,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 261711-20:
(8*2)+(7*6)+(6*1)+(5*7)+(4*1)+(3*1)+(2*2)+(1*0)=110
110 % 10 = 0
So 261711-20-0 is a valid CAS Registry Number.

261711-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-bromo-4-fluoro-phenyl)ethanol

1.2 Other means of identification

Product number -
Other names -

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:261711-20-0 SDS

261711-20-0Relevant articles and documents

α-Oxocarboxylic Acids as Three-Carbon Insertion Units for Palladium-Catalyzed Decarboxylative Cascade Synthesis of Diverse Fused Heteropolycycles

Zhou, Liwei,Qiao, Shujia,Zhou, Fengru,Xuchen, Xinyu,Deng, Guobo,Yang, Yuan,Liang, Yun

supporting information, p. 2878 - 2883 (2021/05/05)

A novel palladium-catalyzed decarboxylative cascade cyclization for the assembly of diverse fused heteropolycycles by employing α-oxocarboxylic acids as three-carbon insertion units is reported. This protocol enables the synthesis of isoquinolinedione- and indolo[2,1-a]isoquinolinone-fused benzocycloheptanones in moderate to good yields by the use of different aryl iodides, including alkene-tethered 2-iodobenzamides and 2-(2-iodophenyl)-1H-indoles. Notably, the approach achieves simultaneous construction of both six- and seven-membered rings via sequential intramolecular carbopalladation, C-H activation, and decarboxylation.

QUINOXALINE DERIVATIVES

-

Page/Page column 79; 80, (2021/07/24)

The present invention relates to compounds according to general formula (I), which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.

Divergent Access to Benzocycles through Copper-Catalyzed Borylative Cyclizations

Yoon, Wan Seok,Han, Jung Tae,Yun, Jaesook

supporting information, p. 4953 - 4959 (2021/09/14)

A copper-catalyzed chemodivergent approach to five- and six-membered benzocycles from dienyl arenes tethered with a ketone has been developed. Through proper choice of coordinating ligands and catalytic conditions, copper-catalyzed borylative cyclization of a single dienyl arene can be diverted to two different pathways, leading to indanols and dihydronaphthalenols with high stereoselectivity. The chiral bidentate bisphosphine ligand (S,S)-Ph-BPE was optimal for asymmetric copper-allyl addition to a tethered ketone via a boat-like transition state, whereas NHC ligands led to boro-allyl addition producing indanols with high diastereoselectivity. (Figure presented.).

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