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121219-03-2

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121219-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121219-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,2,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121219-03:
(8*1)+(7*2)+(6*1)+(5*2)+(4*1)+(3*9)+(2*0)+(1*3)=72
72 % 10 = 2
So 121219-03-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrFO/c7-5-2-1-4(9)3-6(5)8/h1-3,9H

121219-03-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H32488)  4-Bromo-3-fluorophenol, 98%   

  • 121219-03-2

  • 5g

  • 519.0CNY

  • Detail
  • Alfa Aesar

  • (H32488)  4-Bromo-3-fluorophenol, 98%   

  • 121219-03-2

  • 25g

  • 1735.0CNY

  • Detail

121219-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-3-fluorophenol

1.2 Other means of identification

Product number -
Other names 2-fluoro-4-hydroxybromobenzene

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:121219-03-2 SDS

121219-03-2Relevant articles and documents

Planar and distorted indigo as the core motif in novel chromophoric liquid crystals

Porada, Jan H.,Neud?rfl, J?rg-M.,Blunk, Dirk

, p. 8291 - 8301 (2015)

Symmetrically bis-substituted indigo derivatives with long peripheral alkyl chains were synthesised by the reductive condensation of corresponding isatin derivatives. Their thermotropic mesomorphism was investigated with respect to different substitution

Regioselective bromination of arenes mediated by triphosgene-oxidized bromide

Xu, Yingzhou,Hu, Dufen,Zheng, Hui,Mei, David,Gao, Zhaobo

supporting information, (2019/08/30)

This article first time describes triphosgene (BTC) as an oxidant while the non-toxic and easy-to-handle potassium bromide (KBr) as the source of bromine to the bromination reaction of aromatic substrates. The novel brominating protocol gives excellent para-regioselectivity of the alkoxyl/hydroxyl arenes and high yield, offering good potential of commercial scale applications. The mechanism of “Triphosgene oxidize bromide” was proposed.

P-Hydroxyphenacyl photoremovable protecting groups Robust photochemistry despite substituent diversity

Givens, Richard S.,Stensrud, Kenneth,Conrad, Peter G.,Yousef, Abraham L.,Perera, Chamani,Senadheera, Sanjeewa N.,Heger, Dominik,Wirz, Jakob

scheme or table, p. 364 - 384 (2011/06/22)

A broadly based investigation of the effects of a diverse array of substituents on the photochemical rearrangement of p-hydroxyphenacyl esters has demonstrated that common substituents such as F, MeO, CN, CO2R, CONH2, and CH3 have little effect on the rate and quantum efficiencies for the photo-Favorskii rearrangement and the release of the acid leaving group or on the lifetimes of the reactive triplet state. A decrease in the quantum yields across all substituents was observed for the release and rearrangement when the photolyses were carried out in buffered aqueous media at pHs that exceeded the ground-state pKa of the chromophore where the conjugate base is the predominant form. Otherwise, substituents have only a very modest effect on the photoreaction of these robust chromophores.

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