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1-Oxa-4-thiaspiro[4.6]undecane is a cyclic organic compound characterized by a unique structure that includes a spiro junction, which connects two rings in a single molecule. The compound consists of a seven-membered ring with one oxygen atom and a five-membered ring with one sulfur atom. The presence of these heteroatoms (oxygen and sulfur) in the ring system imparts specific chemical properties and reactivity to the molecule. 1-Oxa-4-thiaspiro[4.6]undecane is of interest in organic chemistry due to its potential applications in the synthesis of complex molecules and its unique electronic and steric effects. It is also worth noting that the compound's name, 1-oxa-4-thiaspiro[4.6]undecane, provides a clear indication of its structure, with "1-oxa" indicating the presence of an oxygen atom in the first position and "4-thia" indicating a sulfur atom in the fourth position of the spiro compound, which is part of an undecane (11-carbon) framework.

184-31-6

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184-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184-31-6 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 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 184-31:
(5*1)+(4*8)+(3*4)+(2*3)+(1*1)=56
56 % 10 = 6
So 184-31-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H16OS/c1-2-4-6-9(5-3-1)10-7-8-11-9/h1-8H2

184-31-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Oxa-4-thiaspiro(4.6)undecane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:184-31-6 SDS

184-31-6Downstream Products

184-31-6Relevant academic research and scientific papers

An efficient and chemoselective method for conversion of carbonyl compounds to 1,3-oxathiolanes with 2-mercaptoethanol catalyzed by TiCl 4-montmorillonite

Jin, Tong-Shou,Zhao, Rui-Qiao,Ma, Yan-Ran,Yang, Mi-Na,Guo, Jun-Jie,Li, Tong-Shuang

, p. 503 - 505 (2007/10/03)

Formation of 1,3-oxathiolanes from aldehydes and ketones using 2-mercaptoethanol in the presence of TiCl4-montmorillonite under mild reaction conditions in excellent yields is described. Chemoselective monothioacetalization of aldehyde in the p

Montmorillonite K-10 clay as an efficient solid catalyst for chemoselective protection of carbonyl compounds as oxathiolanes with 2-mercaptoethanol

Gogoi, Siddhartha,Borah, Jagat C.,Barua, Nabin C.

, p. 1592 - 1594 (2007/10/03)

Montmorillonite K-10 clay has been found to be a mild and efficient solid catalyst for the protection of a variety of carbonyl compounds, such as oxathiolanes, with 2-mercaptoethanol in good to excellent yields. In addition, by using this catalyst, high chemoselective protection of aldehydes in presence of ketones has been achieved.

Indium trifluoromethanesulfonate as a mild and chemoselective catalyst for the conversion of carbonyl compounds into 1,3-oxathiolanes

Kazahaya, Kiyoshi,Hamada, Nao,Ito, Shinya,Sato, Tsuneo

, p. 1535 - 1537 (2007/10/03)

An efficient method for the preparation of 1,3-oxathiolanes from aldehydes and ketones with 2-mercaptoethanol in the presence of a catalytic amount of indium trifluoromethanesulfonate is reported.

Zirconium tetrachloride (ZrCl4) as an efficient and chemoselective catalyst for conversion of carbonyl compounds to 1,3-oxathiolanes

Karimi, Babak,Seradj, Hassan

, p. 805 - 806 (2007/10/03)

Different types of aldehydes and ketones can be efficiently converted into their corresponding 1,3-oxathiolanes using 2-mercaptoethanol (1.5-3.2 equiv.) in the presence of catalytic amount (0.04-0.15 equiv.) of ZrCl4 in CH2Cl2/

Interconversion of oxathiolanes and carbonyls under essentially identical conditions

Ravindranathan,Chavan, Subhash P.,Dantale, Shubhada W.

, p. 2285 - 2288 (2007/10/02)

A catalytic, non-aqueous protocol for the interconversion of oxathiolanes and carbonyl compounds at room temperature is described.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Robbe,Fernandez,Dubief,et al.

, p. 235 - 243 (2007/10/02)

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.

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