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912768-78-6

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912768-78-6 Usage

General Description

Tert-butyl 4-(4-methylbenzoyl)piperidine-1-carboxylate is a chemical compound with the molecular formula C20H27NO3. It is a derivative of piperidine, a heterocyclic amine, and contains a tert-butyl group, a benzoyl group, and a carboxylate ester group. tert-Butyl 4-(4-methylbenzoyl)piperidine-1-carboxylate is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential use as a chiral reagent in organic chemistry reactions. Tert-butyl 4-(4-methylbenzoyl)piperidine-1-carboxylate possesses a unique structure and properties that make it valuable in various chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 912768-78-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,7,6 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 912768-78:
(8*9)+(7*1)+(6*2)+(5*7)+(4*6)+(3*8)+(2*7)+(1*8)=196
196 % 10 = 6
So 912768-78-6 is a valid CAS Registry Number.

912768-78-6SDS

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 tert-Butyl 4-(4-methylbenzoyl)piperidine-1-carboxylate

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

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More Details:912768-78-6 SDS

912768-78-6Relevant articles and documents

Direct Aldehyde C-H Arylation and Alkylation via the Combination of Nickel, Hydrogen Atom Transfer, and Photoredox Catalysis

Zhang, Xiaheng,MacMillan, David W. C.

supporting information, p. 11353 - 11356 (2017/08/30)

A mechanism that enables direct aldehyde C-H functionalization has been achieved via the synergistic merger of photoredox, nickel, and hydrogen atom transfer catalysis. This mild, operationally simple protocol transforms a wide variety of commercially available aldehydes, along with aryl or alkyl bromides, into the corresponding ketones in excellent yield. This C-H abstraction coupling technology has been successfully applied to the expedient synthesis of the medicinal agent haloperidol.

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