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1,4-Dithiaspiro[4.4]nonane(7CI,8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

176-39-6

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176-39-6 Usage

Synthesis Reference(s)

Tetrahedron Letters, 31, p. 5815, 1990 DOI: 10.1016/S0040-4039(00)97967-X

Check Digit Verification of cas no

The CAS Registry Mumber 176-39-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 176-39:
(5*1)+(4*7)+(3*6)+(2*3)+(1*9)=66
66 % 10 = 6
So 176-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12S2/c1-2-4-7(3-1)8-5-6-9-7/h1-6H2

176-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dithiaspiro[4.4]nonane

1.2 Other means of identification

Product number -
Other names Cyclopentanon-aethylenthioketal

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:176-39-6 SDS

176-39-6Downstream Products

176-39-6Relevant academic research and scientific papers

Synthetic Methods, III [1]: Sulfated Zirconia Catalyzed Thioacetalization of Carbonyl Compounds

Bandgar,Kasture

, p. 1305 - 1308 (1996)

Sulfated zirconia effectively catalyzes the reaction of carbonyl compounds with 1,2-ethanedithiol or thiophenol to afford the corresponding dithioacetals as useful organosulfur synthons. Isolation of pure products in high yields by simple filtration and e

Ceric Ammonium Nitrate as a Convenient Catalyst for Chemoselective Thioacetalisation

Mandal, Pijus Kumar,Roy, Subhas Chandra

, p. 7823 - 7828 (1995)

A new, mild and chemoselective protection of aldehydes as 1,3-dithiolanes using ceric ammonium nitrate as a catalyst is described.High yields are obtained at room temperature even in the presence of ketones.While alicyclic ketones may also be protected at

A rapid mild and efficient method of thioacetalization using anhydrous iron(III) chloride dispersed on silica gel

Patney

, p. 2259 - 2260 (1991)

Carbonyl compounds are rapidly thioacetalized in near quantitative yields by using anhydrous iron(III) chloride dispersed on silica gel at room temperature.

H-y zeolite, an efficient catalyst for thioacetalization

Kumar, Pradeep,Reddy, Ravinder S.,Singh, Anand P.,Pandey, Bipin

, p. 825 - 826 (1992)

Carbonyl compounds are thioacetalized by 1,2-ethanedithiol in presence of H-Y zeolite in almost quantitative yields (?90%).

Envirocat EPZG(R) as an efficient heterogenous catalyst for thioacetalization of carbonyl compounds

Kasture,Bandgar,Sarkar,Wadgaonkar

, p. 1579 - 1583 (1996)

The reaction of carbonyl compounds with 1,2-ethanedithiol was efficiently catalyzed by Envirocat EPZG(R) to afford the corresponding dithioacetals in excellent yields.

Bis(trimethylsilyl) sulfate-Silica Catalysed Thioacetalisation of Carbonyl Compounds

Patney, Harish K.

, p. 7127 - 7128 (1993)

Bis(trimethylsilyl)sulfate-silica has been shown to be an efficient reagent system for promoting thioacetalisation of carbonyl compounds at room temperature.

Ahydrous Cobalt(II) Bromide Dispersed on Silica Gel: A Mild and Efficient Reagent for Thioacetalisation of Carbonyl Compounds

Patney, Harish K.

, p. 5717 - 5718 (1994)

Anhydrous cobalt(II) bromide dispersed on silica gel has been shown to be a very efficient reagent system for thioacetalisation of a variety of aldehydes and ketones at room temperature.

Zirconium(IV) chloride-silica catalysed thioacetalisation of carbonyl compounds

Patney, Harish K.,Margan, Simon

, p. 4621 - 4622 (1996)

Anhydrous anhydrous zirconium(IV) chloride dispersed on silica gel efficiently thioacetalised a variety of carbonyl compounds in near quantitative yields.

Silica-supported phosphorus pentoxide: A reusable catalyst for S,S-acetalization of carbonyl groups under ambient conditions

Shaterian, Hamid Reza,Azizi, Kobra,Fahimi, Nafiseh

experimental part, p. 85 - 91 (2012/01/06)

Phosphorus pentoxide supported on silica gel (P2O 5/SiO2) efficiently acts as a highly active and reusable catalyst for cyclic and non-cyclic S,S-acetalization of a variety of carbonyl compounds under mild, solvent-free an

Chemoselective dithioacetalization and oxathioacetalization of carbonyl compounds using alumina sulfuric acid as catalyst

Shaterian, Hamid Reza,Hosseinian, Asghar,Ghashang, Majid

experimental part, p. 4097 - 4106 (2009/04/11)

Carbonyl compounds have been successfully converted into their corresponding dithiolane, dithiane, and oxathiolane derivatives using a catalytic amount of alumina sulfuric acid (Al2O3-SO3H) with excellent yields at room temperature in short reaction times under mild conditions. This simple method is a highly chemoselective procedure for protection of aldehydes in the presence of ketones, and the heterogeneous catalyst can be recovered and reused several times without any loss of its activity. Copyright Taylor & Francis Group, LLC.

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