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105873-71-0

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105873-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105873-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,7 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105873-71:
(8*1)+(7*0)+(6*5)+(5*8)+(4*7)+(3*3)+(2*7)+(1*1)=130
130 % 10 = 0
So 105873-71-0 is a valid CAS Registry Number.

105873-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-3-phenyl-1,3-oxazolidine-2-one

1.2 Other means of identification

Product number -
Other names 4-ethyl-3-phenyl-1,3-oxazolidin-2-one

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:105873-71-0 SDS

105873-71-0Downstream Products

105873-71-0Relevant articles and documents

VanadiumV(salen) catalysed synthesis of oxazolidinones from epoxides and isocyanates

Beattie, Christopher,North, Michael

, p. 31345 - 31352 (2014/08/05)

The combination of a vanadiumV(salen) complex V +O(salen) EtOSO3- and tetrabutylammonium bromide forms a highly active catalyst system for the reaction between epoxides and isocyanates leading to oxazolidinones.

Mechanistic studies of tetraphenylstibonium iodide-catalyzed cycloaddition of oxiranes with heterocumulenes

Fujiwara,Baba,Matsuda

, p. 1069 - 1073 (2007/10/02)

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Reduction of Aldehyde with Tributyltin Hydride-HMPA Combined System

Shibata, Ikuya,Yoshida, Tomoyuki,Baba, Akio,Matsuda, Haruo

, p. 619 - 622 (2007/10/02)

Bu3-SnH-HMPA combined system is an efficient reagent for the reduction of aldehydes.The reaction proceeds in good yields, and chemoselective carbonyl reduction is achieved for the substrate which includes another reducible group.Moreover, the intermediate, tin alkoxide, undergoes further reaction such as the preparation of ethers and heterocyclic compounds in the one pot procedure.

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