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9-(1,1-dimethylethyl)-1,5-dioxaspiro[5.5]undecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65156-97-0

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65156-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65156-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65156-97:
(7*6)+(6*5)+(5*1)+(4*5)+(3*6)+(2*9)+(1*7)=140
140 % 10 = 0
So 65156-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O2/c1-12(2,3)11-5-7-13(8-6-11)14-9-4-10-15-13/h11H,4-10H2,1-3H3

65156-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-tert-butyl-1,5-dioxaspiro[5.5]undecane

1.2 Other means of identification

Product number -
Other names EINECS 265-577-5

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:65156-97-0 SDS

65156-97-0Relevant academic research and scientific papers

An efficient procedure for the preparation of cyclic ketals and thioketals catalyzed by zirconium sulfophenyl phosphonate

Curini,Epifano,Marcotullio,Rosati

, p. 1182 - 1184 (2007/10/03)

A convenient method for the preparation of cyclic ketals and thioketals using zirconium sulfophenyl phosphonate as catalyst is described.

The synthesis, stereochemistry and nmr spectra of some new spiro-1,3-dioxanes

Grosu, Ion,Mager, Sorin,Martinez, Roberto,Camacho, Brigida Del Carmen,Plé, Gerard,Mesaros, Clementina

, p. 725 - 733 (2007/10/03)

The stereochemistry of some new spiro-1,3-dioxanes exhibiting axial and helical chirality was investigated using NMR methods. The compounds display semiflexible or anancomeric structures in correlation with the number and type of substituents located on the rings. The influence of the chirality of the spiro skeleton was revealed by the diastereotopicity of protons and carbon atoms.

A DIRECT SYNTHESIS OF CYCLIC ACETALS FROM β- OR γ-HYDROXY EHTHERS BY MEANS OF C-H ACTIVATION

Furuta, Kyoji,Nagata, Takushi,Yamamoto, Hisashi

, p. 2215 - 2218 (2007/10/02)

A direct route to cyclic acetals by means of the remote functionalization promoted by alkoxy radicals is described.

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