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5,6-dimethyl-3a,4,7,7a-tetrahydro-1,3-benzodioxol-2-one is a complex organic compound with a molecular formula of C10H12O3. It is a derivative of benzodioxole, which is a heterocyclic aromatic compound containing both oxygen atoms in its structure. The compound features a tetrahydro ring system, with two methyl groups attached at the 5 and 6 positions, and a carbonyl group at the 2 position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and can be further modified to create a range of derivatives with different properties and uses.

4717-64-0

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4717-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4717-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4717-64:
(6*4)+(5*7)+(4*1)+(3*7)+(2*6)+(1*4)=100
100 % 10 = 0
So 4717-64-0 is a valid CAS Registry Number.

4717-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethyl-3a,4,7,7a-tetrahydro-1,3-benzodioxol-2-one

1.2 Other means of identification

Product number -
Other names 5,6-Dimethyl-(3ar,7ac)-3a,4,7,7a-tetrahydro-benzo[1,3]dioxol-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:4717-64-0 SDS

4717-64-0Relevant academic research and scientific papers

Benzannulation via ruthenium-catalyzed diol-diene [4+2] cycloaddition: One- and two-directional syntheses of fluoranthenes and acenes

Geary, Laina M.,Chen, Te-Yu,Montgomery, T. Patrick,Krische, Michael J.

supporting information, p. 5920 - 5922 (2014/05/20)

A new benzannulation protocol is described and applied to the synthesis of polycyclic aromatic hydrocarbons. Ruthenium(0)-catalyzed diol-diene [4+2] cycloaddition delivers cyclohex-1-ene-4,5-diols, which are subject to aromatization upon dehydration or Nicholas diol deoxydehydration. Employing diol and tetraol reactants, benzannulation can be conducted efficiently in one- and two-directional modes, respectively, as illustrated in the construction of substituted fluoranthenes and acenes.

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