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1211584-76-7

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1211584-76-7 Usage

Description

2-Methoxy-3-(trifluoromethyl)pyridine is a pyridine derivative with the molecular formula C7H6F3NO, featuring a methoxy group and a trifluoromethyl group. It is a versatile chemical compound that holds significant relevance in the fields of chemistry, pharmaceuticals, and biotechnology due to its unique structural features and potential applications.

Uses

Used in Organic Synthesis:
2-Methoxy-3-(trifluoromethyl)pyridine is utilized as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its distinctive structure allows it to serve as a useful intermediate in the production of a wide range of compounds.
Used in Chemical Reactions:
2-methoxy-3-(trifluoromethyl)pyridine is employed as a reagent in chemical reactions, contributing to the synthesis of diverse molecules and facilitating various chemical processes.
Used in Pharmaceutical Industry:
2-Methoxy-3-(trifluoromethyl)pyridine is used as a precursor in the development of new pharmaceuticals, thanks to its unique structural elements that can be incorporated into drug molecules to enhance their properties and effectiveness.
Used in Biotechnology:
Ongoing research is exploring the potential of 2-Methoxy-3-(trifluoromethyl)pyridine as a therapeutic agent for various medical applications, capitalizing on its interesting biological activities.
Used in Agrochemical Industry:
2-methoxy-3-(trifluoromethyl)pyridine is also used in the agrochemical sector for the synthesis of various agrochemicals, leveraging its structural features to improve the performance of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 1211584-76-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,8 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1211584-76:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*8)+(3*4)+(2*7)+(1*6)=127
127 % 10 = 7
So 1211584-76-7 is a valid CAS Registry Number.

1211584-76-7SDS

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 3-?Pyridinamine, 6-?methoxy-?5-?(trifluoromethyl)?-

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:1211584-76-7 SDS

1211584-76-7Downstream Products

1211584-76-7Relevant articles and documents

NOVEL PYRAZOLO PYRIMIDINE DERIVATIVES AND THEIR USE AS MALT1 INHIBITORS

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Page/Page column 78; 79, (2015/12/31)

The present invention describes new pyrazolo-pyrimidine derivatives of formula (I) or a pharmaceutically acceptable salt thereof; (I) wherein, R1 is halogen, cyano, or C1-C3alkyl optionally substituted by halogen; R2 is C1-C6alkyl optionally substituted one or more times by C1-C6alkyl, C2-C6alkenyl, hydroxyl, N,N-di-C1-C6alkyl amino, N-mono-C1-C6alkyl amino, O-Rg, Rg, phenyl, or by C1-C6alkoxy wherein said alkoxy again may optionally be substituted by C1-C6alkoxy, N,N-di-C1-C6alkyl amino, Rg or phenyl; C3-C6cycloalkyl optionally substituted by C1-C6alkyl, N,N-di-C1-C6alkyl amino or C1-C6alkoxy-C1-C6alkyl, and/or two of said optional substituents together with the atoms to which they are bound may form an annulated or spirocyclic 4 - 6 membered saturated heterocyclic ring comprising 1 - 2 O atoms; phenyl optionally substituted by C1-C6alkoxy; a 5 - 6 membered heteroaryl ring having 1 to 3 heteroatoms selected from N and O said ring being optionally substituted by C1-C6alkyl which may be optionally substituted by amino or hydroxy; Rg; or N,N-di-C1-C6alkyl amino carbonyl; and R is phenyl independently substituted two or more times by Ra, 2-pyridyl independently substituted one or more times by Rb, 3-pyridyl independently substituted one or more times by Rc, or 4-pyridyl independently substituted one or more times by Rd; which are generally interacting with MALT1 proteolytic and/or autoproteolytic activity, and in particular which may inhibit said activity. The present invention further describes the synthesis of said new pyrazolo-pyrimidine derivatives, their use as a medicament, especially by interacting with MALT1 proteolytic and/or autoproteolytic activity.

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