Welcome to LookChem.com Sign In|Join Free

CAS

  • or

345-72-2

Post Buying Request

345-72-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

345-72-2 Usage

General Description

ETHYL 3-FLUORO-4-METHOXYBENZOYLFORMATE is a chemical compound with the molecular formula C11H11FO4. It is also known as ethyl 3-fluoro-4-methoxybenzoylformate. ETHYL 3-FLUORO-4-METHOXYBENZOYLFORMATE is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is often employed in organic synthesis as a reagent for the preparation of various functionalized aromatic compounds. ETHYL 3-FLUORO-4-METHOXYBENZOYLFORMATE is a colorless liquid with a sweet odor and is considered to be a potentially hazardous substance that should be handled with care and in accordance with safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 345-72-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 345-72:
(5*3)+(4*4)+(3*5)+(2*7)+(1*2)=62
62 % 10 = 2
So 345-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11FO4/c1-3-16-11(14)10(13)7-4-5-9(15-2)8(12)6-7/h4-6H,3H2,1-2H3

345-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(3-fluoro-4-methoxyphenyl)-2-oxoacetate

1.2 Other means of identification

Product number -
Other names Ethyl 3-fluoro-4-methoxybenzoylformate

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:345-72-2 SDS

345-72-2Relevant articles and documents

Selective Acylation of Aryl- A nd Heteroarylmagnesium Reagents with Esters in Continuous Flow

Heinz, Benjamin,Djukanovic, Dimitrije,Ganiek, Maximilian A.,Martin, Benjamin,Schenkel, Berthold,Knochel, Paul

supporting information, p. 493 - 496 (2020/01/31)

A selective acylation of readily accessible organomagnesium reagents with commercially available esters proceeds at convenient temperatures and short residence times in continuous flow. Flow conditions allow us to prevent premature collapse of the hemiacetal intermediates despite noncryogenic conditions, thus furnishing ketones in good yields. Throughout, the coordinating ability of the ester and/or Grignard was crucial for the reaction outcome. This was leveraged by the obtention of several bisaryl ketones using 2-hydroxy ester derivatives as substrates.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 345-72-2