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Dihydro-5-methyl-5-(3-methylbutyl)furan-2(3H)-one is a complex organic compound with the molecular formula C10H18O2. It is a derivative of furan, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. The compound features a dihydro structure, which means it has two hydrogen atoms added to the furan ring, and a 3-methylbutyl group attached to the 5-position of the ring. This results in a more stable and less reactive molecule compared to its parent furan. The compound has potential applications in the synthesis of various pharmaceuticals, fragrances, and other chemical products due to its unique structure and properties.

3285-02-7

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3285-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3285-02-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3285-02:
(6*3)+(5*2)+(4*8)+(3*5)+(2*0)+(1*2)=77
77 % 10 = 7
So 3285-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-8(2)4-6-10(3)7-5-9(11)12-10/h8H,4-7H2,1-3H3

3285-02-7SDS

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 5-methyl-5-(3-methylbutyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 5-isopentyl-5-methyl-dihydro-furan-2-one

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:3285-02-7 SDS

3285-02-7Downstream Products

3285-02-7Relevant academic research and scientific papers

Cooperative Polar/Steric Strategy in Achieving Site-Selective Photocatalyzed C(sp3)?H Functionalization

Yamada, Keiichi,Fukuyama, Takahide,Fujii, Saki,Ravelli, Davide,Fagnoni, Maurizio,Ryu, Ilhyong

supporting information, p. 8615 - 8618 (2017/06/30)

Synergistic control over the SH2 transition states of hydrogen abstraction exploiting polar and steric effects provides a promising cooperative strategy for site-selective C(sp3)?H functionalization using decatungstate anion photocatalysis. By using this photocatalytic approach, the C?H bonds of substituted lactones and cyclic ketones were functionalized selectively. In the remarkable case of 2-isoamyl 4-tert-butyl cyclohexanone (1 t) bearing five methyl, five methylene, and three methine C?H bonds, one methine C?H bond in the isoamyl tether was selectively functionalized.

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