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2-oxohexahydro-2H-3,5-methanocyclopenta[b]furan-7-carboxylic acid is a complex organic compound with the molecular formula C8H12O4. It is a derivative of cyclopenta[b]furan, featuring a carboxylic acid group at the 7-position, a ketone group at the 2-position, and a methyl bridge between the 3 and 5 positions. This molecule is characterized by its unique ring structure and functional groups, which may contribute to its potential applications in various chemical or pharmaceutical contexts. The compound's specific properties, such as solubility, reactivity, and stability, would depend on the conditions under which it is synthesized and stored.

4582-20-1

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4582-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4582-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4582-20:
(6*4)+(5*5)+(4*8)+(3*2)+(2*2)+(1*0)=91
91 % 10 = 1
So 4582-20-1 is a valid CAS Registry Number.

4582-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-oxo-4-oxatricyclo[4.2.1.03,7]nonane-9-carboxylic acid

1.2 Other means of identification

Product number -
Other names Bromocyclen

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:4582-20-1 SDS

4582-20-1Relevant academic research and scientific papers

A total synthesis of (±)-hop ether

Lin, Ching-Han,Su, Yi-Lin,Tai, Huo-Mu

, p. 771 - 777 (2007/10/03)

A total synthesis of the iridoid monoterpene (±)-hop ether (2) is described. The Norrish I type fragmentation of bicyclo[2.2.1]heptone (5) is the key step.{A figure is presented}.

Acid-catalysed Lactonisation and Iodolactonisation of Norbornene-carboxylic Acids

Sadikun, Amirin bin,Davies, David I.

, p. 2461 - 2466 (2007/10/02)

The acid-catalysed lactonisation of 3-(norborn-5-en-2-yl)propionic acid and 4-(norborn-5-en-2-yl)butyric acid affords 3-(2-exo-hydroxynorborn-2-endo-yl)propionic acid spiro-γ-lactone and 4-(2-exo-hydroxynorborn-2-endo-yl)butyric acid spiro-δ-lactone, resp

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