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17060-81-0

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17060-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17060-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,6 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17060-81:
(7*1)+(6*7)+(5*0)+(4*6)+(3*0)+(2*8)+(1*1)=90
90 % 10 = 0
So 17060-81-0 is a valid CAS Registry Number.

17060-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-bromo-2,6-dimethylphenyl)-2-(diethylamino)acetamide

1.2 Other means of identification

Product number -
Other names 4'-Bromo-2-(diethylamino)-2',6'-acetoxylidide

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:17060-81-0 SDS

17060-81-0Downstream Products

17060-81-0Relevant articles and documents

Photocatalytic Oxidative Bromination of Electron-Rich Arenes and Heteroarenes by Anthraquinone

Petzold, Daniel,K?nig, Burkhard

supporting information, p. 626 - 630 (2017/11/22)

The estimated excited oxidation potential of sodium anthraquinone-2-sulfonate (SAS) increases from 1.8 V to about 2.3 V vs SCE by protonation with Br?nsted acids. This increased photooxidation power of protonated anthraquinone was used for the regio-selective oxidative bromination of electron rich (hetero)arenes and drugs in good yield. The mild reaction conditions are compatible with many functional groups, such as double and triple bonds, ketones, amides and amines, hydroxyl groups, carboxylic acids and carbamates. Mechanistic investigations indicate the photooxidation of the arene followed by nucleophilic bromide addition as the likely pathway. (Figure presented.).

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