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Ethyl 2,2-dimethyl-4-oxo-3,4-dihydro-2H-pyran-6-carboxylate is a complex organic compound with the chemical formula C10H14O4. It is a derivative of pyran, a heterocyclic compound containing a six-membered ring with one oxygen atom. This specific compound features a carboxylate group at the 6-position, a 4-oxo group, and two methyl groups at the 2-position. It is a colorless liquid with a fruity odor and is used as a synthetic intermediate in the production of various fragrances and flavorings. Due to its complex structure, it is typically synthesized through multi-step chemical reactions and is not found naturally. The compound is also known for its potential applications in the pharmaceutical industry, although further research is needed to explore its full potential.

5464-36-8

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5464-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5464-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5464-36:
(6*5)+(5*4)+(4*6)+(3*4)+(2*3)+(1*6)=98
98 % 10 = 8
So 5464-36-8 is a valid CAS Registry Number.

5464-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,2-dimethyl-4-oxo-3H-pyran-6-carboxylate

1.2 Other means of identification

Product number -
Other names HMS3089H04

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:5464-36-8 SDS

5464-36-8Relevant academic research and scientific papers

Metal-Free Visible Light-Mediated Photocatalysis: Controlling Intramolecular [2 + 2] Photocycloaddition of Enones through Axial Chirality

Clay, Anthony,Vallavoju, Nandini,Krishnan, Retheesh,Ugrinov, Angel,Sivaguru, Jayaraman

, p. 7191 - 7200 (2016)

Atropisomeric enone-imides and enone-amides featuring N-CAryl bond rotation were evaluated for intramolecular [2 + 2] photocycloaddition. Straight addition product was observed over cross-addition product with good control over reactivity. The atropselectivity was found to be dependent on the substituent on the aryl ring. Substitution-dependent atropselectivity was rationalized on the basis of a divergent mechanistic pathway.

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