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10552-10-0

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10552-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10552-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10552-10:
(7*1)+(6*0)+(5*5)+(4*5)+(3*2)+(2*1)+(1*0)=60
60 % 10 = 0
So 10552-10-0 is a valid CAS Registry Number.

10552-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-piperidin-1-ylbenzamide

1.2 Other means of identification

Product number -
Other names 4-Piperidino-benzoesaeureamid

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:10552-10-0 SDS

10552-10-0Relevant articles and documents

General Paradigm in Photoredox Nickel-Catalyzed Cross-Coupling Allows for Light-Free Access to Reactivity

Nocera, Daniel G.,Qin, Yangzhong,Sun, Rui

supporting information, p. 9527 - 9533 (2020/04/08)

Self-sustained NiI/III cycles are established as a potentially general paradigm in photoredox Ni-catalyzed carbon–heteroatom cross-coupling reactions through a strategy that allows us to recapitulate photoredox-like reactivity in the absence of light across a wide range of substrates in the amination, etherification, and esterification of aryl bromides, the latter of which has remained, hitherto, elusive under thermal Ni catalysis. Moreover, the accessibility of esterification in the absence of light is especially notable because previous mechanistic studies on this transformation under photoredox conditions have unanimously invoked energy-transfer-mediated pathways.

Solid phase synthesis of aryl amines

Willoughby, Christopher A.,Chapman, Kevin T.

, p. 7181 - 7184 (2007/10/03)

A method for the solid phase synthesis of aryl amines is reported. The method involves a palladium mediated coupling reaction between aryl bromides and amines. The products are isolated in high purity and good yields. This method should prove to be a useful tool for constructing combinatorial libraries containing the aryl amine moiety.

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