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202865-66-5

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202865-66-5 Usage

Chemical Properties

Colorless liquid

Uses

2-Bromo-5-fluorobenzyl alcohol is used as intermediates in pharmaceutical and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 202865-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,8,6 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 202865-66:
(8*2)+(7*0)+(6*2)+(5*8)+(4*6)+(3*5)+(2*6)+(1*6)=125
125 % 10 = 5
So 202865-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrFN.ClH/c8-7-2-1-6(9)3-5(7)4-10;/h1-3H,4,10H2;1H

202865-66-5 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H61596)  2-Bromo-5-fluorobenzyl alcohol, 97%   

  • 202865-66-5

  • 1g

  • 439.0CNY

  • Detail
  • Alfa Aesar

  • (H61596)  2-Bromo-5-fluorobenzyl alcohol, 97%   

  • 202865-66-5

  • 5g

  • 1758.0CNY

  • Detail

202865-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-5-fluorophenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-Bromo-5-fluorobenzyl alcohol

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:202865-66-5 SDS

202865-66-5Relevant articles and documents

Benzoxaborole-1-alcohol compound and preparation method and application thereof

-

Paragraph 0078-0084, (2020/06/24)

The invention belongs to the field of bactericides, and particularly relates to a benzoxaborole-1-alcohol compound and a preparation method and application thereof. The benzoxaborole-1-alcohol compound has good bactericidal activity, can effectively control tomato early blight, wheat scab, rice sheath blight disease, strawberry gray mold, apple blotch, cucumber anthracnose and other crop diseases,can produce excellent antibacterial effects at low concentration, and shows good selectivity. The compound is used as a leucyl-tRNA synthetase inhibitor, the evolution difference of aminoacyl-tRNA synthetase of germs and eukaryotes is utilized, and the compound has very high safety to non-target organisms while killing the germs and can be used as a bactericide in agriculture.

Metal- and Hydride-Free Pentannulative Reductive Aldol Reaction

Satpathi, Bishnupada,Dutta, Lona,Ramasastry

supporting information, p. 170 - 174 (2019/01/04)

Traditionally, the reductive aldol reaction is a metal-catalyzed and hydride-promoted coupling between enones and aldehydes. We present a phosphine-mediated diastereoselective intramolecular reductive aldol reaction of α-substituted dienones and aldehydes, which is metal-free and hydride-free. The synthetic utility of the reductive aldol adducts is demonstrated by elaborating them in one step to indeno[1,2-b]furanones, indeno[1,2-b]pyrans, and dibenzo[a,h]azulen-8-ones.

Indolone derivative as well as preparation method and application thereof

-

Paragraph 0268-0269, (2019/07/04)

The invention relates to a compound represented by formula (A) or a pharmaceutically acceptable salt, a stereoisomer, a tautomer, a polymorphic substance, a solvate, a metabolite or a prodrug thereof,and also relates to a pharmaceutical composition containing the compound. The compound can be used for treating cancer or immune system diseases.

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