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2527-99-3

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2527-99-3 Usage

Chemical Properties

White to slightly yellow crystalline powder

Uses

It is used in the preparation of hydroquinone bis(2-carbomethoxy-5-furyl ether).

Check Digit Verification of cas no

The CAS Registry Mumber 2527-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2527-99:
(6*2)+(5*5)+(4*2)+(3*7)+(2*9)+(1*9)=93
93 % 10 = 3
So 2527-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrO3/c1-9-6(8)4-2-3-5(7)10-4/h2-3H,1H3

2527-99-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B20524)  Methyl 5-bromo-2-furoate, 97%   

  • 2527-99-3

  • 1g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (B20524)  Methyl 5-bromo-2-furoate, 97%   

  • 2527-99-3

  • 5g

  • 1370.0CNY

  • Detail
  • Alfa Aesar

  • (B20524)  Methyl 5-bromo-2-furoate, 97%   

  • 2527-99-3

  • 25g

  • 3487.0CNY

  • Detail

2527-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-bromofuran-2-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 5-Bromo-2-furoate

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:2527-99-3 SDS

2527-99-3Relevant articles and documents

Nitronium Acetate Adducts of Furan Derivatives

Balina, Gisela,Kesler, Patricia,Petre, Janet,Pham, Dung,Vollmar, Arnulf

, p. 3811 - 3818 (2007/10/02)

An improved procedure for the isolation of the main addition products of the reaction between nitronium acetate and furfural diacetate or methyl 2-furoate is described.The kinetics of the deacetylation of the diastereomeric 1,4-adducts in buffer solutions revealed a substantial primary hydrogen isotope effect.Mild acid-induced alcoholysis transformed the adducts into 2,5-dialkoxy-2,5-dihydrofurans.The reaction chemistry of the furan adducts is compared with the solvolytic pathways reported for ipso nitronium acetate adducts formed from alkylbenzenes.

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