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4,5-dibromo-5-methyldihydrofuran-2(3H)-one is a chemical compound characterized by its unique structure and properties. It is a heterocyclic compound, specifically a dihydrofuran derivative, with a molecular formula of C5H6Br2O2. The compound features a five-membered dihydrofuran ring, which includes one oxygen atom and four carbon atoms. Two bromine atoms are attached to the 4th and 5th positions of the ring, while a methyl group is present at the 5th position as well. The compound has a 3H-configuration, indicating that it has three hydrogen atoms in a specific arrangement. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique reactivity and structural features.

1424-35-7

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1424-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1424-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1424-35:
(6*1)+(5*4)+(4*2)+(3*4)+(2*3)+(1*5)=57
57 % 10 = 7
So 1424-35-7 is a valid CAS Registry Number.

1424-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dibromo-5-methyloxolan-2-one

1.2 Other means of identification

Product number -
Other names 4,5-Dibrom-5-methyl-dihydro-furan-2-on

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:1424-35-7 SDS

1424-35-7Upstream product

1424-35-7Relevant academic research and scientific papers

STUDIES ON STRUCTURALLY SIMPLE α,β-BUTENOLIDES-I NEW SYNTHESIS OF RACEMIC γ-HYDROXYMETHYL-α,β-BUTENOLIDE AND DERIVATIVES

Cardellach, J.,Estopa, C.,Font, J.,Moreno-Manas, M.,Ortuno, R. M.,et al.

, p. 2377 - 2394 (2007/10/02)

Exhaustive approaches to the synthesis of racemic γ-heterosubstituted γ-methyl-α,β-butenolides are presented, starting from C3 synthons (glyceraldehyde, glycidaldehyde, acrolein and 2,3-epoxypropyl ethers).Good general methods for the preparation of γ-hydroxymethyl-α,β-butenolide 2, several of its ether derivatives, as well as of γ-bromomethyl-α,β-butenolide 5, are given.The reactivities of these structurally simple but highly functionalized compounds, convenient synthons for more complex molecules, are preliminarily explored.

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