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5661-50-7

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5661-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5661-50-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5661-50:
(6*5)+(5*6)+(4*6)+(3*1)+(2*5)+(1*0)=97
97 % 10 = 7
So 5661-50-7 is a valid CAS Registry Number.

5661-50-7SDS

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-phenoxyacetamide

1.2 Other means of identification

Product number -
Other names N-Acetyl-O-phenyl-hydroxylamin

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:5661-50-7 SDS

5661-50-7Relevant articles and documents

Cobalt(III)-Catalyzed Enantioselective Intermolecular Carboamination by C?H Functionalization

Ozols, Kristers,Onodera, Shunsuke,Wo?niak, ?ukasz,Cramer, Nicolai

, p. 655 - 659 (2020/12/01)

High-valent cyclopentadienyl cobalt catalysis is a versatile tool for sustainable C?H bond functionalizations. To harness the full potential of this strategy, control of the stereoselectivity of these processes is necessary. Herein, we report highly enant

Synthesis of ortho-phenolic sulfilimines via an intermolecular sulfur atom transfer cascade reaction

Ren, Yan,Song, Yinan,Xiong, Feng,Xu, Shaojian,Zhang, Linxing,Zhang, Xinhao,Zuo, Yingying

, p. 3799 - 3803 (2020/06/08)

To expand the toolbox for the synthesis of ortho-phenolic sulfilimines, sigmatropic rearrangements were introduced to the field of sulfilimine chemistry. Herein we report a N-H sulfenylation/[2,3]-sigmatropic rearrangement cascade reaction. This mild reaction enables commercially available thiols to serve as the sulfenylation reagent and generates water as the sole byproduct. Moreover, the reaction has a wide substrate scope and can be conducted on a gram scale with excellent reaction efficiency.

An internal oxidant-directing strategy enabling transition metal-free C–S bond ligation

Zuo, Yingying,Xiong, Feng,Zhao, Jing

, p. 4174 - 4179 (2019/05/24)

Organic sulfur compounds have broad applications in biology, medicine and material sciences and intensive efforts have been devoted to developing mild and general C–S bond-forming methods. However, a mild, transition-metal-free, direct C–H bond functionalization method remains elusive. Here, we report the use of an internal oxidant-directing strategy to achieve this goal. The cascade reactions described here show excellent chemoselectivity and a wide substrate scope for both oxyamines and sulfenylation reagents. This study enlarges the synthesis toolbox for preparing structurally diverse sulfilimines under mild conditions.

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