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884494-81-9

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884494-81-9 Usage

Uses

3-Bromo-5-fluoro-2-methoxypyridine is a compound used in the synthesis of 5-Fluoro-2-methoxy-3-(2R)-2-pyrrolidinylpyridine (1213093-30-1).

Check Digit Verification of cas no

The CAS Registry Mumber 884494-81-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,4,9 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 884494-81:
(8*8)+(7*8)+(6*4)+(5*4)+(4*9)+(3*4)+(2*8)+(1*1)=229
229 % 10 = 9
So 884494-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrFNO/c1-10-6-5(7)2-4(8)3-9-6/h2-3H,1H3

884494-81-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H64915)  3-Bromo-5-fluoro-2-methoxypyridine, 95%   

  • 884494-81-9

  • 250mg

  • 206.0CNY

  • Detail
  • Alfa Aesar

  • (H64915)  3-Bromo-5-fluoro-2-methoxypyridine, 95%   

  • 884494-81-9

  • 1g

  • 617.0CNY

  • Detail
  • Alfa Aesar

  • (H64915)  3-Bromo-5-fluoro-2-methoxypyridine, 95%   

  • 884494-81-9

  • 5g

  • 2470.0CNY

  • Detail

884494-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-5-fluoro-2-methoxypyridine

1.2 Other means of identification

Product number -
Other names 3-BROMO-5-FLUORO-2-METHOXYPYRIDINE

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:884494-81-9 SDS

884494-81-9Relevant articles and documents

Synthesis process of 2-methoxy-3-bromo-5-fluoropyridine

-

, (2021/03/06)

The invention discloses a synthesis process of 2-methoxy-3-bromo-5-fluoropyridine, which comprises the following steps: dissolving 2-methoxy-5-aminopyridine in an acid, adding nitrous acid or nitriteto prepare a diazotized intermediate state, reacting with a fluorinating reagent to obtain 2-methoxy-5-fluoropyridine, and carrying out a bromination reaction process on 2-methoxy-5-fluoropyridine anda bromination reagent to obtain 2-methoxy-3-bromo-5-fluoropyridine. The synthesis process provided by the invention has the advantages of cheap and easily available raw materials, mild reaction conditions, high yield, easiness in industrial production and the like.

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