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3,3-dimethylfuran-2,4(3H,5H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5436-15-7

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5436-15-7 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 15, p. 572, 1950 DOI: 10.1021/jo01149a021Tetrahedron Letters, 28, p. 1039, 1987

Check Digit Verification of cas no

The CAS Registry Mumber 5436-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5436-15:
(6*5)+(5*4)+(4*3)+(3*6)+(2*1)+(1*5)=87
87 % 10 = 7
So 5436-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O3/c1-6(2)4(7)3-9-5(6)8/h3H2,1-2H3

5436-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyloxolane-2,4-dione

1.2 Other means of identification

Product number -
Other names EINECS 226-604-6

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:5436-15-7 SDS

5436-15-7Downstream Products

5436-15-7Relevant academic research and scientific papers

Method for Synthesis of 2,5-Dioxane-1,4-Diones

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Page/Page column 3, (2008/06/13)

The invention relates to a novel method for the synthesis of 2,5-dioxane-1,4-diones having formula (I), comprising the oxidation of the ketone function of a cyclic compound having formula (II), wherein R1, R2, R3 and R4 independently represent the hydrogen atom, halo, (C2-C6) alkenyl, (C3-C7)cycloalkyl, cyclohexenyl and a radical having formula —(CH2)m—V—W.

THE ACID CATALYZED CYCLIZATION OF DIAZOKETONES: PREPARATION OF 2,4(3H,5H)FURANDIONES

Miller, R. D.,Theis, W.

, p. 1039 - 1042 (2007/10/02)

Diazoketones derived from substituted ethyl hydrogen malonates produced by the selective hydrolysis of the corresponding malonate esters cyclize in the presence of catalytic amounts of boron trifluoride etherate in methanol to yield 2,4(3H,5H)furandiones.The cyclic keto orthoesters appear to be intermediates in the reaction.

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