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907208-89-3

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  • 4-(5-Methyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester

    Cas No: 907208-89-3

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907208-89-3 Usage

Uses

Used in Pharmaceutical Industry:
4-(5-Methyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester, 98+% C15H23N3O2, MW: 277.36 is used as an intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(5-Methyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester, 98+% C15H23N3O2, MW: 277.36 is utilized as a key component in the production of agrochemicals, such as pesticides and herbicides, due to its ability to enhance the effectiveness and selectivity of these compounds.
Used in Organic Synthesis:
4-(5-Methyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester, 98+% C15H23N3O2, MW: 277.36 serves as a valuable building block in organic synthesis, allowing for the creation of a wide range of organic compounds with diverse applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 907208-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,7,2,0 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 907208-89:
(8*9)+(7*0)+(6*7)+(5*2)+(4*0)+(3*8)+(2*8)+(1*9)=173
173 % 10 = 3
So 907208-89-3 is a valid CAS Registry Number.

907208-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(5-methylpyridin-2-yl)piperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 4-(5-methyl-2-pyridyl)piperazinecarboxylate

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:907208-89-3 SDS

907208-89-3Relevant articles and documents

Remarkably Efficient Iridium Catalysts for Directed C(sp2)-H and C(sp3)-H Borylation of Diverse Classes of Substrates

Chattopadhyay, Buddhadeb,Hassan, Mirja Md Mahamudul,Hoque, Md Emdadul

supporting information, p. 5022 - 5037 (2021/05/04)

Here we describe the discovery of a new class of C-H borylation catalysts and their use for regioselective C-H borylation of aromatic, heteroaromatic, and aliphatic systems. The new catalysts have Ir-C(thienyl) or Ir-C(furyl) anionic ligands instead of the diamine-type neutral chelating ligands used in the standard C-H borylation conditions. It is reported that the employment of these newly discovered catalysts show excellent reactivity and ortho-selectivity for diverse classes of aromatic substrates with high isolated yields. Moreover, the catalysts proved to be efficient for a wide number of aliphatic substrates for selective C(sp3)-H bond borylations. Heterocyclic molecules are selectively borylated using the inherently elevated reactivity of the C-H bonds. A number of late-stage C-H functionalization have been described using the same catalysts. Furthermore, we show that one of the catalysts could be used even in open air for the C(sp2)-H and C(sp3)-H borylations enabling the method more general. Preliminary mechanistic studies suggest that the active catalytic intermediate is the Ir(bis)boryl complex, and the attached ligand acts as bidentate ligand. Collectively, this study underlines the discovery of new class of C-H borylation catalysts that should find wide application in the context of C-H functionalization chemistry.

A class of GPR40 agonist compounds with amide structure, and uses thereof

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Paragraph 0145; 0146; 0147; 0148; 0150, (2019/05/02)

The present invention relates to a class of amide compounds with a novel structure, and a pharmaceutical composition thereof, wherein the structure of the amide compound is represented by a general formula (I). According to the present invention, the amide compound (I) can regulate GPR40 activity, and can be used for GPR40 activity related diseases such as diabetes and metabolic syndrome. The formula I is defined in the specification.

SULFONIC ACID SALTS OF HETEROCYCLYLAMIDE-SUBSTITUTED IMIDAZOLES

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Paragraph 0148-0154, (2014/10/29)

The invention relates to sulfonic acid salts of heterocyclylamide-substituted imidazoles, and to solvates and hydrates thereof, to the use thereof for treating and/or preventing diseases, and to use thereof for producing drugs for treating and/or preventi

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