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2-methyl-2-(6-methylhept-6-enyl)-1,3-dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40632-70-0

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40632-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40632-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40632-70:
(7*4)+(6*0)+(5*6)+(4*3)+(3*2)+(2*7)+(1*0)=90
90 % 10 = 0
So 40632-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-11(2)7-5-4-6-8-12(3)13-9-10-14-12/h1,4-10H2,2-3H3

40632-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-2-(6-methylhept-6-enyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 2-methyl-2-(6-methyl-hept-6-enyl)-[1,3]dioxolane

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:40632-70-0 SDS

40632-70-0Downstream Products

40632-70-0Relevant academic research and scientific papers

Synthesis of Substituted Cyclooctanols by a Samarium(II) Iodide Promoted 8-Endo Radical Cyclization Process

Molander, Gary A.,McKie, Jeffrey A.

, p. 3186 - 3192 (2007/10/02)

Samarium(II) iodide (SmI2) has been employed to promote an efficient 8-endo radical cyclization reaction of a variety of substituted olefinic ketones.Various substituted monocyclic, fused bicyclic, and bridged bicyclic cyclooctanols have been synthesized in fair to excellent yield via this protocol.In addition to delineating the synthetic potential of this reaction, experiments have been conducted to determine the source of reduced, noncyclized byproducts present in this and related SmI2-mediated reactions performed under protic conditions.

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