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O,O'-dibenzoyl-2,3-bis(hydroxylamino)-2,3-dimethylbutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82365-28-4

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82365-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82365-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,6 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82365-28:
(7*8)+(6*2)+(5*3)+(4*6)+(3*5)+(2*2)+(1*8)=134
134 % 10 = 4
So 82365-28-4 is a valid CAS Registry Number.

82365-28-4SDS

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 O,O'-dibenzoyl-2,3-bis(hydroxylamino)-2,3-dimethylbutane

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82365-28-4 SDS

82365-28-4Downstream Products

82365-28-4Relevant academic research and scientific papers

Direct N-O bond formation via oxidation of amines with benzoyl peroxide

Banerjee, Amit,Yamamoto, Hisashi

, p. 2124 - 2129 (2019/02/20)

Herein, we report a general and efficient method for direct N-O bond formation without undesirable C-N bond (amide) formation starting from commercially available amines and benzoyl peroxide. The oxidation of 1,2-diamines to furnish bis-(benzoyloxy)-1,2-diamines is reported for the first time. We found that a significant amount of water (BPO?:?water = 3?:?1) in combination with Cs2CO3 is necessary to achieve high selectivity and yield. The reaction conditions are applicable to a wide range of 1,2-diamine and 1,2-disubstituted-1,2-diamine substrates. Additionally this method is highly applicable to primary and secondary amines. Further, the present method can access chiral bis-hydroxamic acids and bis-hydroxyl amines in just two steps from 1,2-diamines. The reaction conditions are simple, mild and inert atmosphere free. The synthetic potential of this methodology is further demonstrated in the short synthesis of a chiral BHA ligand.

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