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699016-24-5

699016-24-5

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699016-24-5 Usage

Chemical Properties

light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 699016-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,9,0,1 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 699016-24:
(8*6)+(7*9)+(6*9)+(5*0)+(4*1)+(3*6)+(2*2)+(1*4)=195
195 % 10 = 5
So 699016-24-5 is a valid CAS Registry Number.
InChI:InChI=1S/C8H7FO2/c1-11-8-3-6(5-10)2-7(9)4-8/h2-5H,1H3

699016-24-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H32415)  3-Fluoro-5-methoxybenzaldehyde, 98%   

  • 699016-24-5

  • 250mg

  • 764.0CNY

  • Detail

  • Alfa Aesar

  • (H32415)  3-Fluoro-5-methoxybenzaldehyde, 98%   

  • 699016-24-5

  • 1g

  • 2136.0CNY

  • Detail

699016-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Fluoro-5-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-FLUORO-M-ANISALDEHYDE

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:699016-24-5 SDS

699016-24-5Downstream Products

699016-24-5Relevant articles and documents

Copper-Mediated Fluorination of Aryl Trisiloxanes with Nucleophilic Fluoride

Dorel, Ruth,Boehm, Philip,Schwinger, Daniel P.,Hartwig, John F.

supporting information, p. 1759 - 1762 (2020/02/05)

A method for the nucleophilic fluorination of heptamethyl aryl trisiloxanes to form fluoroarenes is reported. The reaction proceeds in the presence of Cu(OTf)2 and KHF2 as the fluoride source under mild conditions for a broad range of heptamethyltrisiloxyarenes with high functional group tolerance. The combination of this method with the silylation of aryl C?H bonds enables the regioselective fluorination of non-activated arenes controlled by steric effects following a two-step protocol.

Sanglifehrin Derivatives and Methods for Their Production

-

Paragraph 0157; 0158, (2014/04/03)

There are provided inter alia compounds of formula (I) and (II) and their use in therapy, particularly for the treatment of viral infection.

NOVEL DOSAGE FORM

-

Page/Page column 63, (2013/05/21)

There is provided inter alia apharmaceutical dosage form fororal administration comprising a sanglifehrin as active ingredient in which the sanglifehrin active ingredient is protected from acid degradation in the stomach environment following oral adminis

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