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692058-21-2

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692058-21-2 Usage

General Description

Tert-butyl 4-(2,2,2-trifluoroethyl)piperazine-1-carboxylate is a chemical compound with the molecular formula C13H22F3N3O2. It is a piperazine derivative that contains a tert-butyl group and a trifluoroethyl group. tert-butyl 4-(2,2,2-trifluoroethyl)piperazine-1-carboxylate is often used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and therapeutic agents. It is also used in organic chemistry as a building block for the creation of more complex molecules. Tert-butyl 4-(2,2,2-trifluoroethyl)piperazine-1-carboxylate is a colorless to light yellow liquid and should be handled and stored with proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 692058-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,0,5 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 692058-21:
(8*6)+(7*9)+(6*2)+(5*0)+(4*5)+(3*8)+(2*2)+(1*1)=172
172 % 10 = 2
So 692058-21-2 is a valid CAS Registry Number.

692058-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(2,2,2-trifluoroethyl)piperazine-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

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

More Details:692058-21-2 SDS

692058-21-2Relevant articles and documents

An Improved Stereocontrolled Access Route to Piperidine or Azepane β-Amino Esters and Azabicyclic β- and γ-Lactams; Synthesis of Novel Functionalized Azaheterocyles

Ouchakour, Lamiaa,Nonn, Melinda,Remete, Attila M.,Kiss, Loránd

, p. 3874 - 3885 (2021/06/16)

An improved, efficient synthesis of some functionalized saturated azaheterocycles has been accomplished by controlled functionalization of various readily available cyclic compounds containing ring C=C bond. The stereocontrolled synthetic concept was based on the oxidative ring cleavage of various unsaturated scaffolds across ozonolysis followed by ring closing with double reductive amination with primary alkylamines or fluorinated alkylamines. The protocol provided versatile azaheterocyclic derivatives with a piperidine or azepane framework.

SUBSTITUTED PYRAZOLE COMPOUNDS AND METHODS OF USING THEM FOR TREATMENT OF HYPERPROLIFERATIVE DISEASES

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Paragraph 236, (2018/06/21)

Disclosed are compounds useful, for example, in methods of treating hyperproliferative disorders such as cancer, methods of arresting the cell cycle in cancer cells, methods of inhibiting glutathione synthesis in cancer cells, and associated compounds for

BIS-HETEROARYL DERIVATIVES AS MODULATORS OF PROTEIN AGGREGATION

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Paragraph 0122, (2017/02/24)

The present invention relates to certain bis-heteroaryl compounds, pharmaceutical compositions containing them, and methods of using them, including methods for preventing, reversing, slowing, or inhibiting protein aggregation, and methods of treating diseases that are associated with protein aggregation, including neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, Lewy body disease, Parkinson's disease with dementia, fronto- temporal dementia, Huntington's Disease, amyotrophic lateral sclerosis, and multiple system atrophy, and cancer including melanoma.

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