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1,3-Dioxolane, 2-[2,6-dimethyl-7-(phenylsulfonyl)-5-heptenyl]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90165-64-3

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90165-64-3 Usage

Explanation

The name describes the structure of the compound, including the dioxolane ring, the heptenyl group, and the (Z)configuration.

Explanation

The dioxolane ring is a four-membered ring with two oxygen atoms, while the heptenyl group is a seven-carbon chain with a double bond.

Explanation

The compound's stability allows it to be used as a building block in the synthesis of more complex organic molecules without easily breaking down.

Explanation

The compound's ability to undergo different types of reactions makes it a valuable tool in organic synthesis.

Explanation

Due to its stability and versatility, 1,3-Dioxolane, 2-[2,6-dimethyl-7-(phenylsulfonyl)-5-heptenyl]-, (Z)- is often used as a starting material or intermediate in the production of various drugs and agricultural chemicals.

Explanation

These functional groups contribute to the compound's reactivity and its ability to participate in various chemical reactions.

Explanation

Stereochemistry refers to the spatial arrangement of atoms in a molecule, which can affect its properties and reactivity. In this case, the (Z)configuration determines the relative positions of the substituents on the double bond.

Molecular Structure

Contains a dioxolane ring and a heptenyl group.

(Z)Configuration

Indicates a cis configuration of the double bond.

Stability

Known for its stability in various chemical reactions.

Versatility

Can participate in a variety of chemical reactions.

Applications

Commonly used in organic synthesis and as a precursor for pharmaceuticals and agrochemicals.

Functional Groups

Dioxolane ring, heptenyl group, phenylsulfonyl group, and a double bond.

Stereochemistry

The compound exhibits stereochemistry due to the presence of a double bond and the (Z)configuration.

Check Digit Verification of cas no

The CAS Registry Mumber 90165-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,6 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90165-64:
(7*9)+(6*0)+(5*1)+(4*6)+(3*5)+(2*6)+(1*4)=123
123 % 10 = 3
So 90165-64-3 is a valid CAS Registry Number.

90165-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((Z)-7-Benzenesulfonyl-2,6-dimethyl-hept-5-enyl)-[1,3]dioxolane

1.2 Other means of identification

Product number -
Other names -

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:90165-64-3 SDS

90165-64-3Downstream Products

90165-64-3Relevant academic research and scientific papers

Reaction of isopulegol and similar alcohols with sulfuryl chloride

Bulliard, M.,Balme, G.,Monteiro, N.,Gore, J.

, p. 222 - 231 (2007/10/02)

The reaction of isopulegol with sulfuryl chloride (or chlorine) gives two types of products: on one hand 8-chlorocitronellal and 6-chloroisocitronellal both issued from a fragmentation pathway and, on the other hand 10-chloroisopulegol resulting from an allylic chlorination.The first process, the radical nature of which is demonstrated, is clearly favored by elevated temperatures while the second one is exclusive at 0 deg C.Homologous compounds such as p-mentha-1,8-dien-5-ols, 3-phenylisopulegol and isopulegone dioxolane give rise to one or both of these processes. --- Key Words: allylic chlorination / radical fragmentation

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