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828246-28-2

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828246-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828246-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,2,4 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 828246-28:
(8*8)+(7*2)+(6*8)+(5*2)+(4*4)+(3*6)+(2*2)+(1*8)=182
182 % 10 = 2
So 828246-28-2 is a valid CAS Registry Number.

828246-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-5-hydroxy-3-methyl-4H-1,4-benzoxazin-2-one

1.2 Other means of identification

Product number -
Other names 2H-1,4-Benzoxazin-2-one,3-ethyl-3,4-dihydro-5-hydroxy-3-methyl

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:828246-28-2 SDS

828246-28-2Downstream Products

828246-28-2Relevant academic research and scientific papers

Reactive ketimino radical acceptors: Intermolecular alkyl radical addition to imines with a phenolic hydroxyl group

Miyabe, Hideto,Yamaoka, Yousuke,Takemoto, Yoshiji

, p. 2099 - 2106 (2007/10/03)

Intermolecular carbon radical addition to the carbon-nitrogen double bond of ketimines was studied. In the study on the reactivity of various aldimines, we found that the aldimine 7 having a phenolic hydroxyl group shows an excellent reactivity toward nuc

Aqueous medium radical addition to ketimines with a phenolic hydroxyl group

Miyabe, Hideto,Yamaoka, Yousuke,Takemoto, Yoshiji

, p. 2597 - 2599 (2007/10/03)

Intermolecular alkyl radical addition to ketimines having 2-phenolic hydroxyl group proceeded effectively in aqueous media, providing the novel method for construction of all-substituted sp3-hybridized carbon center.

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