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3-butyl-4-methylfuran-2,5-dione is a chemical compound with the molecular formula C9H12O3. It is a derivative of furan-2,5-dione, which is characterized by a five-membered ring containing two oxygen atoms and a double bond. The compound features a butyl group (a four-carbon chain) attached to the third carbon of the furan ring and a methyl group (a single carbon) attached to the fourth carbon. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is an example of a heterocyclic compound, which are often found in natural products and have a wide range of biological activities.

7541-33-5

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7541-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7541-33-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7541-33:
(6*7)+(5*5)+(4*4)+(3*1)+(2*3)+(1*3)=95
95 % 10 = 5
So 7541-33-5 is a valid CAS Registry Number.

7541-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-4-methylfuran-2,5-dione

1.2 Other means of identification

Product number -
Other names butyl-methyl-maleic acid anhydride

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:7541-33-5 SDS

7541-33-5Downstream Products

7541-33-5Relevant academic research and scientific papers

Preparation of Disubstituted Maleic Anhydrides from Reactive 2-Oxo-3H-imidazopyridinium Compounds

Baumann, Marcus E.,Bosshard, Hans,Breitenstein, Werner,Rist, Guenter

, p. 396 - 403 (1986)

A new useful method for the preparation of disubstituted maleic anhydrides, most of them bearing additional functional groups in the side chain, is described.The key step of the synthesis consists of the addition of 2-oxo-3H-imidazopyridinium compounds to a variety of different Michael acceptors.

A New Approach to Rethrolone Synthesis

Jondiko, Isaac J. O.,Pattenden, Gerald

, p. 467 - 470 (2007/10/02)

Rearrangement of the 4-ylidenebutenolides (4) and (5), with sodium methoxide in methanol, leads to the cyclopent-2-ene-1,4-diones (6), which when heated with sodium chloride in dimethyl sulphoxide give the 1,4-diones (7).The latter can be reduced using zinc in acetic acid, to the dihydroethrolones (8).In a similar manner, rearrangement of (10) produces (11a) which can be demethoxycarbonylated to (11b), an intermediate used previously in a synthesis of natural jasmololone (8; R = EtCH:CH).

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