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Ethyl (octylsulfonyl)acetate is a chemical compound with the molecular formula C12H24O4S. It is an ester derivative of octylsulfonyl acetic acid, characterized by the presence of an octylsulfonyl group attached to the acetate moiety. This organic compound is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure provides unique reactivity and selectivity in chemical reactions, making it a valuable building block in the development of new compounds with specific properties and applications.

2850-20-6

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2850-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2850-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2850-20:
(6*2)+(5*8)+(4*5)+(3*0)+(2*2)+(1*0)=76
76 % 10 = 6
So 2850-20-6 is a valid CAS Registry Number.

2850-20-6SDS

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 2-octyl tetrahydropyran-2-yl ether

1.2 Other means of identification

Product number -
Other names 2-tetrahydropyranyl ether of 2-octanol

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:2850-20-6 SDS

2850-20-6Relevant academic research and scientific papers

Efficient synthesis of aliphatic sulfones by Mg mediated coupling reactions of sulfonyl chlorides and aliphatic halides

Fu, Ying,Xu, Qin-Shan,Li, Quan-Zhou,Du, Zhengyin,Wang, Ke-Hu,Huang, Danfeng,Hu, Yulai

supporting information, p. 2841 - 2845 (2017/04/03)

Sulfonyl chlorides were reduced to anhydrous sulfinate salts with magnesium under sonication. These sulfinates were alkylated to sulfones with alkyl chlorides in the presence of catalytic sodium iodide under sonication. A variety of aliphatic sulfones was efficiently prepared by this one-pot two-step procedure.

Design and synthesis of stable α-diazo-β-oxo sulfoxides

Collins, Stuart G.,O'Sullivan, Orlagh C. M.,Kelleher, Patrick G.,Maguire, Anita R.

, p. 1706 - 1725 (2013/03/29)

Diazo transfer adjacent to a sulfoxide moiety to provide stable, isolable α-diazo-β-oxo sulfoxides has been achieved. Use of monocyclic and bicyclic sulfoxide precursors is critical in enabling isolation of stable derivatives, through introduction of conformational constraint, while acyclic α-diazo-β-oxo sulfoxides are too labile to isolate and characterize.

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