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817195-71-4

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817195-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 817195-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,1,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 817195-71:
(8*8)+(7*1)+(6*7)+(5*1)+(4*9)+(3*5)+(2*7)+(1*1)=184
184 % 10 = 4
So 817195-71-4 is a valid CAS Registry Number.

817195-71-4SDS

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 1-(furan-2-yl)-N-(4-methylphenyl)methanimine oxide

1.2 Other means of identification

Product number -
Other names Benzenamine,N-(2-furanylmethylene)-4-methyl-,N-oxide (9CI)

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:817195-71-4 SDS

817195-71-4Downstream Products

817195-71-4Relevant articles and documents

Water-Soluble Maleimide-Modified Gold Nanoparticles (AuNPs) as a Platform for Cycloaddition Reactions

Ghiassian, Sara,Gobbo, Pierangelo,Workentin, Mark S.

, p. 5438 - 5447 (2015/08/24)

Maleimide-terminated triethylene glycol thiolate monolayer-protected gold nanoparticles (Mal-EG4-AuNPs) with a core size of 2.5±0.7 nm were prepared. Mal-EG4-AuNPs were modified in high yields via interfacial 1,3-dipolar cycloadditio

Magnesium iodide promoted reactions of nitrones with cyclopropanes: A synthesis of tetrahydro-1,2-oxazines

Ganton, Michael D.,Kerr, Michael A.

, p. 8554 - 8557 (2007/10/03)

Anhydrous magnesium iodide (MgI2) is shown to be an effective promoter of the "homo 3+2" dipolar cycloaddition of nitrones with 1,1-cyclopropane diesters. In almost all cases the products tetrahydro-1,2-oxazines are formed in excellent yields. The reactions are highly diastereoselective for a cis relationship between the substitutents at the 3- and 6-positions on the tetrahydrooxazine ring. As an alternative to using a preformed nitrone, the reaction may be performed in a 3-component sense by combining an aldehyde, an hydroxylamine, and the cyclopropane in the presence of catalytic MgI2.

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