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5-Chloro-3-methylpyridine-2-carbonitrile is a pyridine derivative with the molecular formula C7H5ClN2, featuring a chlorine atom and a nitrile group attached to the carbon atom in the 2-position of the pyridine ring. It is a versatile chemical compound that has garnered attention in the scientific community for its diverse synthetic applications.

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  • 156072-84-3 Structure
  • Basic information

    1. Product Name: 5-Chloro-3-methylpyridine-2-carbonitrile
    2. Synonyms: 5-Chloro-3-methylpyridine-2-carbonitrile;5-Chloro-2-cyano-3-methylpyridine, 5-Chloro-3-methylpicolinonitrile;5-Chloro-3-Methylpicolinonitrile
    3. CAS NO:156072-84-3
    4. Molecular Formula: C7H5ClN2
    5. Molecular Weight: 153
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156072-84-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Chloro-3-methylpyridine-2-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Chloro-3-methylpyridine-2-carbonitrile(156072-84-3)
    11. EPA Substance Registry System: 5-Chloro-3-methylpyridine-2-carbonitrile(156072-84-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 156072-84-3(Hazardous Substances Data)

156072-84-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
5-Chloro-3-methylpyridine-2-carbonitrile is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a valuable building block for the development of new drugs and pesticides.
Used in Organic Synthesis:
5-Chloro-3-methylpyridine-2-carbonitrile is used as a building block in organic synthesis, particularly in the production of heterocyclic compounds. Its versatile reactivity and functional group compatibility allow for the creation of a wide range of complex organic molecules.
Used in Materials Science:
5-Chloro-3-methylpyridine-2-carbonitrile has potential applications in the field of materials science. Its unique properties may contribute to the development of new materials with specific characteristics, such as improved stability or reactivity.
Used as a Reagent in Chemical Research:
5-Chloro-3-methylpyridine-2-carbonitrile is also used as a reagent in chemical research. Its diverse synthetic applications make it a valuable tool for scientists exploring new chemical reactions and pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 156072-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,0,7 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 156072-84:
(8*1)+(7*5)+(6*6)+(5*0)+(4*7)+(3*2)+(2*8)+(1*4)=133
133 % 10 = 3
So 156072-84-3 is a valid CAS Registry Number.

156072-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-3-methylpicolinonitrile

1.2 Other means of identification

Product number -
Other names 5-chloro-3-methylpyridine-2-carbonitrile

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:156072-84-3 SDS

156072-84-3Relevant articles and documents

CYCLOPROPYL FUSED THIAZIN-2-AMINE COMPOUNDS AS BETA-SECRETASE INHIBITORS AND METHODS OF USE

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Page/Page column 294; 295, (2016/04/20)

The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula (I): wherein variables A4, A5, A6, A8, and each of Ra, Rb, R1, R2, R3 and R7 of Formula (I), independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and 15 deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimers Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formulas (II) and (III), and sub-formula embodiments thereof, intermediates and methods for preparing compounds of the invention.

BRIDGED BICYCLIC AMINO THIAZINE DIOXIDE COMPOUNDS AS INHIBITORS OF BETA-SECRETASE AND METHODS OF USE THEREOF

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Paragraph 0993, (2015/02/19)

The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula I: wherein variables A4, A5, A6, A8, R1, R2, R3, R7 and n of Formula I, independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and corresponding uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formula II and sub-formula embodiments thereof, compounds of Formula III, intermediates and processes and methods useful for the preparation of compounds of Formulas I-III, and sub-Formulas thereof.

PERFLUORINATED CYCLOPROPYL FUSED 1,3-OXAZIN-2-AMINE COMPOUNDS AS BETA-SECRETASE INHIBITORS AND METHODS OF USE

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Page/Page column 143, (2014/09/29)

PERFLUORINATED CYCLOPROPYL FUSED 1,3-OXAZIN-2-AMINE COMPOUNDS AS BETA-SECRETASE INHIBITORS AND METHODS OF USE ABSTRACT OF THE DISCLOSURE The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula I: {INSERT STRUCTURE HERE} I wherein variables A4, A5, A6, A8, each of Ra, Rb, R1, R2, R3 and R7 of Formula I, independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formulas II and III, and sub-formula embodiments thereof, intermediates and methods for preparing compounds of the invention.

PERFLUORINATED 5,6-DIHYDRO-4H-1,3-OXAZIN-2-AMINE COMPOUNDS AS BETA-SECRETASE INHIBITORS AND METHODS OF USE

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Page/Page column, (2014/09/16)

The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula I: wherein variables A4, A5, A6, A8, each of R1 and R2, R3 and R7 of Formula I, independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and corresponding uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formulas II and III, and sub-formula embodiments thereof, intermediates and processes and methods useful for the preparation of compounds of Formulas I-III.

3,5-Disubstituted-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof

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, (2008/06/13)

Disclosed are 3,5-disubstituted-[1,2,4]-oxadiazoles and analogs thereof, represented by the Formula I: wherein Ar1, R2, A, B and D are defined herein. The present invention relates to the discovery that compounds having Formula I are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention may be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

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