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185-70-6

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185-70-6 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 92, p. 5753, 1970 DOI: 10.1021/ja00722a047Organic Syntheses, Coll. Vol. 5, p. 755, 1973

Check Digit Verification of cas no

The CAS Registry Mumber 185-70-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 185-70:
(5*1)+(4*8)+(3*5)+(2*7)+(1*0)=66
66 % 10 = 6
So 185-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O/c1-2-4-7(5-3-1)6-8-7/h1-6H2

185-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Oxaspiro[2.5]octane

1.2 Other means of identification

Product number -
Other names 1-Oxa-spiro[2.5]octan

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:185-70-6 SDS

185-70-6Relevant articles and documents

Revisiting the Corey-Chaykovsky reaction: The solvent effect and the formation of β-hydroxy methylthioethers

Peng, Yu,Yang, Jin-Hui,Li, Wei-Dong Z.

, p. 1209 - 1215 (2007/10/03)

The classical Corey-Chaykovsky (CC) reaction of ketones in ethereal solvents (i.e., THF or Et2O) resulted in the production of a significant amount of β-hydroxy methylthioether 2 along with normal epoxide product 1. Some interesting and synthet

OXYDATION D'ALCENES CYCLIQUES PAR L'IODYLBENZENE CATALYSEE PAR L'ACETYLACETONATE DE VANADYLE

Barret, R.,Pautet, F.,Daudon, M.,Mathian, B.

, p. 439 - 440 (2007/10/02)

Iodylbenzene with vanadyl acetylacetonate oxidizes cyclic alkenes, the experimental results accord with a free radical oxidation mechanism.

Preparative Oxidation of Cycloalkanes with O(3P) Atoms. Microwave Discharge of CO2 as a Source of O(3P) Atoms.

Zadok, Elazar,Mazur, Yehuda

, p. 2223 - 2225 (2007/10/02)

Reaction of O atoms produced by CO2 discharge with cycloalkanes leads to their hydroxy, keto, and epoxy derivatives.The main products of oxidation of isomeric 1,2-dimethylcyclohexanes and cis-decalin were their respective tertiary alcohols formed with a high retention of configuration.This oxidation proceeds via radical mechanism, and the alcohols are formed by radical combination in a solvent cage.The influence of temperature and of O2 on the relative product distribution was investigated.

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