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ethyl 3-bromofuran-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 32460-07-4 Structure
  • Basic information

    1. Product Name: ethyl 3-bromofuran-2-carboxylate
    2. Synonyms: ethyl 3-bromofuran-2-carboxylate
    3. CAS NO:32460-07-4
    4. Molecular Formula: C7H7BrO3
    5. Molecular Weight: 219.03268
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 32460-07-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl 3-bromofuran-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 3-bromofuran-2-carboxylate(32460-07-4)
    11. EPA Substance Registry System: ethyl 3-bromofuran-2-carboxylate(32460-07-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 32460-07-4(Hazardous Substances Data)

32460-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32460-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,4,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32460-07:
(7*3)+(6*2)+(5*4)+(4*6)+(3*0)+(2*0)+(1*7)=84
84 % 10 = 4
So 32460-07-4 is a valid CAS Registry Number.

32460-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-bromofuran-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Furancarboxylic acid,3-bromo-,ethyl ester

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:32460-07-4 SDS

32460-07-4Relevant articles and documents

SUBSTITUTED TETRAHYDROFURANS AS MODULATORS OF SODIUM CHANNELS

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Paragraph 00969-00970, (2021/06/11)

Compounds, and pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels are provided. Also provided are pharmaceutical compositions comprising the compounds or pharmaceutically acceptable salts and methods of using the compounds, pharmaceutically acceptable salts, and pharmaceutical compositions in the treatment of various disorders, including pain.

HETEROCYCLIC COMPOUND AND USE THEREOF

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Paragraph 0599, (2013/06/05)

The present invention aims to provide a compound having a PDE inhibitory action and useful as a medicament for the prophylaxis or treatment of schizophrenia and the like. A compound represented by the formula (1x): wherein each symbol is as des

Regio- and chemoselective C-H chlorination/bromination of electron-deficient arenes by weak coordination and study of relative directing-group abilities

Sun, Xiuyun,Shan, Gang,Sun, Yonghui,Rao, Yu

supporting information, p. 4440 - 4444 (2013/05/22)

It's all relative: A practical and efficient PdII-catalyzed regio- and chemoselective chlorination/bromination has been developed for the facile synthesis of a broad range of aromatic chlorides. The reaction demonstrates excellent reactivity, good functional-group tolerance, and high yields. A preliminary study was conducted to evaluate relative directing-group abilities of various functionalities. Copyright

2-FURANCARBOXYLIC ACID HYDRAZIDES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME

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Page 29, (2008/06/13)

The present invention provides 2-furancarboxylic acid hydrazide compounds represented by General Formula(I) below, and prodrugs, physiologically acceptable salts, hydrates, solvates thereof, methods for producing them and pharmaceutical compositions containing them: wherein A is a group represented by Formula (a) or the like: (wherein either R4 or R5 represents cyano, nitro or the like, and the other represents a hydrogen atom or the like); either R1 or R2 represents a group: -D-(X)m-R6 or the like, and the other represents a group: -E-(Y)n-R7, hydrogen atom, aryl or the like; R3 is a hydrogen atom or the like; D and E independently represent aryl; X and Y independently represent 0 or the like; R6 and R7 independently represent alkyl, aryl, arylalkyl or the like; and m and n are independently 0 or 1, provided that the aryl is optionally substituted. Such compounds exhibit a potent antagonistic activity on glucagon receptor and are of use as preventive and/or therapeutic agents for symptoms and diseases in which glucagon is involved.

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