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679391-85-6

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679391-85-6 Usage

Type of compound

Spiro compound

Definition of spiro compound

Contains two non-adjacent carbon atoms connected by two different rings

Presence of ethyl groups

Two

Presence of methyl groups

Two

Attachment of ethyl and methyl groups

Attached to the non-carbon atoms of the rings

Physical state at room temperature

Colorless liquid

Common uses

Solvent and reagent in organic synthesis

Potential applications

Pharmaceutical and chemical industries

Additional potential

Building block for the synthesis of more complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 679391-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,9,3,9 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 679391-85:
(8*6)+(7*7)+(6*9)+(5*3)+(4*9)+(3*1)+(2*8)+(1*5)=226
226 % 10 = 6
So 679391-85-6 is a valid CAS Registry Number.

679391-85-6SDS

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 8,8-diethyl-2,2-dimethyl-1,7-dioxaspiro[4.4]nonane

1.2 Other means of identification

Product number -
Other names 8,8-Diethyl-2,2-dimethyl-1,7-dioxa-spiro[4.4]nonane

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:679391-85-6 SDS

679391-85-6Relevant articles and documents

Regioselective synthesis of 1,7-dioxaspiro[4.4]nonanes from a trimethylenemethane dianion synthon

Alonso, Francisco,Dacunha, Bruno,Meléndez, Jaisiel,Yus, Miguel

, p. 3437 - 3450 (2007/10/03)

2-Chloromethyl-3-(2-methoxyethoxy)prop-1-ene behaves as a versatile trimethylenemethane dianion synthon, precursor of a variety of methylidenic diols obtained by DTBB-catalysed lithiation in the presence of a carbonyl compound (E1=R1R2CO) in THF at -78 to 0°C, followed by the addition of an epoxide [E2=R3R 4C(O)CHR5] at 0 to 20°C and final hydrolysis. These diols undergo double intramolecular iodoetherification in the presence of iodine and silver(I) oxide in THF or dioxane-water, to give the corresponding 1,7-dioxaspiro[4.4]nonanes, which can be easily oxidised to a variety of 1,7-dioxaspiro[4.4]nonan-6-ones. These skeletons are present in a wide series of natural products.

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