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1,3-Dioxolane, 2-methyl-2-[3-(phenylthio)propyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97600-68-5

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97600-68-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

It is classified as an organic compound because it contains carbon and hydrogen atoms bonded together.

Explanation

The compound has a cyclic structure, which means its atoms are arranged in a closed ring.

Explanation

A common name is a widely recognized name for a chemical compound, often derived from its structure or properties.

Explanation

Due to its chemical properties, 1,3-Dioxolane, 2-methyl-2-[3-(phenylthio)propyl]is used as a solvent in various industrial applications.

Explanation

The compound's structure consists of a dioxolane ring (a four-membered ring with two oxygen atoms) and a phenylthio group (a phenyl group bonded to a sulfur atom).

Explanation

The compound's unique structure and properties make it useful for various applications in the chemical industry.

Explanation

Proper handling and management of the compound are necessary to minimize potential health and environmental risks.

Explanation

Specific safety measures for handling and storage of the compound are not mentioned in the material provided. However, it is generally advised to follow standard safety protocols for handling chemicals, such as wearing personal protective equipment and using proper ventilation.

Classification

Organic compound

Cyclic structure

Yes

Uses

Solvent in adhesives, coatings, and cleaning agents

Chemical structure

Dioxolane ring and phenylthio group

Applications

Chemical industry

Health and environmental risks

Caution required

Safety measures

Not provided

Check Digit Verification of cas no

The CAS Registry Mumber 97600-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,0 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97600-68:
(7*9)+(6*7)+(5*6)+(4*0)+(3*0)+(2*6)+(1*8)=155
155 % 10 = 5
So 97600-68-5 is a valid CAS Registry Number.

97600-68-5SDS

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 2-methyl-2-(3-phenylsulfanylpropyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane,2-methyl-2-[3-(phenylthio)propyl]

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:97600-68-5 SDS

97600-68-5Relevant academic research and scientific papers

Ring contraction of cyclobutanes and a novel cascade reaction: Application to synthesis of (±)-anthoplalone and (±)-lepidozene

Ihara,Taniguchi,Tokunaga,Fukumoto

, p. 8092 - 8100 (2007/10/02)

Two efficient and practical synthetic methodologies for the construction of small ring systems have been developed. The first method involves a novel rearrangement of cyclobutanes 10 and 14 leading to cyclopropanes 11 and 15 employing BF3·OEts

SYNTHESIS OF SINGLE ISOMERS (E OR Z) OF PROTECTED γ,δ-UNSATURATED KETONES BY THE HORNER-WITTIG REACTION

Cornish Christopher A.,Warren, Stuart

, p. 2585 - 2598 (2007/10/02)

The lithium derivative of the γ-diphenylphosphinoyl ketal (10a) added to aldehydes and ketones to give stable Horner-Wittig intermediates (11) which were separated and converted into single isomers (E or Z) or γ,δ-unsaturated ketals (12). erythro-Adducts (11) and hence Z-(12), were selectively formed by addition of aldehydes and threo adducts (11), and hence E-(12), by reduction of the corresponding α-diphenylphosphinoyl ketones (13), prepared by acylation of the same γ-diphenylphosphinoyl ketal (10a).

Photochemistry of 3-Acylated and 3-Allylated 3-Methyloxepin-2(3H)-ones

Hoshi, Nobuto,Uda, Hisashi

, p. 925 - 945 (2007/10/02)

The photolysis of 3-acetyl- and 3-benzoyl-3-methyloxepin-2(3H)-ones has been shown to produce the products through an initial 1,5-acetyl or -benzoyl shift.

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