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2-Acetyl-3-Chloropyridine is a heterocyclic compound with a basic unit of pyridine, characterized by its molecular formula C7H6ClNO. It is a member of pyridines and an acyl chloride, and its chloropyridine functional group gives it unique chemical behaviors. 2-ACETYL-3-CHLOROPYRIDINE is predominantly used as a reactive intermediate in various chemical synthesis processes and in pharmaceutical formulations. Due to its reactivity, it requires careful handling and specific storage conditions to maintain stability.

131109-75-6

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131109-75-6 Usage

Uses

Used in Chemical Synthesis:
2-Acetyl-3-Chloropyridine is used as a reactive intermediate for the synthesis of various chemical compounds. Its unique functional group allows for versatile reactions, making it a valuable component in the creation of new molecules.
Used in Pharmaceutical Formulations:
2-Acetyl-3-Chloropyridine is used as a key component in the development of pharmaceutical drugs. Its reactivity and unique properties contribute to the formulation of new medications, potentially leading to advancements in the treatment of various medical conditions.
Used in Research and Development:
2-Acetyl-3-Chloropyridine is employed as a research compound in the study of heterocyclic chemistry and its applications. Its unique properties and reactivity make it an interesting subject for scientific exploration, potentially leading to new discoveries and innovations in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 131109-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131109-75:
(8*1)+(7*3)+(6*1)+(5*1)+(4*0)+(3*9)+(2*7)+(1*5)=86
86 % 10 = 6
So 131109-75-6 is a valid CAS Registry Number.

131109-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chloropyridin-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(3-chloropyridin-2-yl)ethanone

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:131109-75-6 SDS

131109-75-6Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND

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Paragraph 1261-1262, (2019/02/19)

A compound represented by formula (I) or an N-oxide compound thereof is provided with excellent control efficacies against harmful arthropods, wherein A1 represents a nitrogen atom or a CR4;R4 represents a hydrogen atom, a

HETEROCYCLIC COMPOUND

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Paragraph 0587; 0588, (2019/05/15)

A compound of formula (I), or an N-oxide thereof is provided. In the compound of formula (I), Het1 represents Het1-1, Het1-2, Het1-3, Het1-4, Het1-5, Het1-6, Het1-7, H

HETEROCYCLIC COMPOUND

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Paragraph 0661; 0662, (2019/04/25)

Provided is a compound of formula (I) or an N-oxide thereof, wherein Het1 represents Het1-1, Het1-2, Het1-3, Het1-4 or Het1-5, and the remaining variable groups are as defined in the specification. The compound of formula (I) or N-oxide compound thereof has an excellent control effect against arthropod pests.

PEST CONTROL COMPOSITION AND APPLICATIONS THEREOF

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Paragraph 0178, (2017/05/02)

PROBLEM TO BE SOLVED: To provide a pest control composition having excellent efficacy of pest control. SOLUTION: A pest control composition comprises a compound represented by formula (1) and one or more compounds selected from group (a) or group (b). [In the formula, each symbol represents definition described in the specification.] SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

PYRIDAZINE COMPOUND

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Paragraph 0639, (2017/11/07)

A pyridazine compound represented by formula (1): wherein A represents a nitrogen atom or a CR6, R1 represents a C2-C10 alkyl group having one or more halogen atoms, etc., R2 and R3 represent independently of each other a hydrogen atom, etc., R4 represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, R5 represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, etc., R6 represents a hydrogen atom, etc., n represents 0, 1, or 2, and p represents 0, 1, or 2, has an excellent efficacy for controlling harmful arthropods.

PYRIMIDINONE COMPOUND

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Paragraph 0621, (2017/11/10)

A pyrimidinone compound represented by formula (1): wherein: A1 represents a nitrogen atom or a CR4; A2 represents a nitrogen atom and A3 represents a CR3b, or A2 represents a CR3a and A3 represents a nitrogen atom; Q represents an oxygen atom or a sulfur atom; G represents a C2-C10 chain hydrocarbon group having one or more halogen atoms, etc.; R1 represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms; R2 represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, etc.; R4 represents a hydrogen atom, etc.; R3, R3a, and R3b represent independently of each other a hydrogen atom, etc.; n represents 0, 1, or 2; and p represents 0, 1, 2, or 3 has an excellent efficacy for controlling harmful arthropods.

GUANIDINE COMPOUNDS, AND USE THEREOF AS BINDING PARTNERS FOR 5-HT5 RECEPTORS

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Page/Page column 101, (2010/02/13)

The invention relates to guanidine compounds of general formula (I), corresponding enantiomeric, diastereomeric, and/or tautomeric forms thereof, and pharmaceutically acceptable salts thereof. The invention further relates to the use of guanidine compounds as binding partners for 5-HT5 receptors in order to treat diseases modulated by 5-HT5 receptor activity, especially treat neurodegenerative and neuropsychiatric disorders and the signs, symptoms, and malfunctions associated therewith.

SUBSTITUTED BICYCLIC QUINAZOLIN-4-YLAMINE DERIVATIVES

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Page/Page column 57, (2010/02/11)

Substituted bicyclic quinazolin-4-ylamine derivatives are provided. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with patholog

Substituted (7-pyridyl-4-phenylamino-quinazolin-2-yl)-methanol analogues

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Page/Page column 19, (2010/02/14)

Substituted (7-pyridyl-4-phenylamino-quinazolin-2-yl)-methanol analogues are provided. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions assoc

2-SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS CAPSAICIN RECEPTOR MODULATORS

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Page 68, (2010/02/07)

Certain 2-substituted quinazolin-4-ylamine analogues are provided. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with pathologi

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