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3-Chloro-5-methoxyaniline is an organic compound that serves as a key intermediate in the synthesis of various pharmaceutical products. It is characterized by the presence of a chloro substituent at the 3-position and a methoxy group at the 5-position on the aniline backbone, which contributes to its reactivity and potential applications in medicinal chemistry.

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  • 10272-06-7 Structure
  • Basic information

    1. Product Name: 3-chloro-5-methoxyaniline
    2. Synonyms: 3-chloro-5-methoxyaniline;Einecs 233-614-4;3-chloro-5-Methoxy-benzenaMine;3-Chloro-5-aminoanisole
    3. CAS NO:10272-06-7
    4. Molecular Formula: C7H8ClNO
    5. Molecular Weight: 157.59752
    6. EINECS: 233-614-4
    7. Product Categories: N/A
    8. Mol File: 10272-06-7.mol
  • Chemical Properties

    1. Melting Point: 33 °C
    2. Boiling Point: 280.3°Cat760mmHg
    3. Flash Point: 123.3°C
    4. Appearance: /
    5. Density: 1.234g/cm3
    6. Vapor Pressure: 0.00381mmHg at 25°C
    7. Refractive Index: 1.572
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: Chloroform (Slightly), Methanol (Slightly)
    10. PKA: 3.12±0.10(Predicted)
    11. Stability: Hygroscopic
    12. CAS DataBase Reference: 3-chloro-5-methoxyaniline(CAS DataBase Reference)
    13. NIST Chemistry Reference: 3-chloro-5-methoxyaniline(10272-06-7)
    14. EPA Substance Registry System: 3-chloro-5-methoxyaniline(10272-06-7)
  • 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: 10272-06-7(Hazardous Substances Data)

10272-06-7 Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-5-methoxyaniline is used as a synthetic intermediate for the preparation of a range of pharmaceutical goods. Its unique chemical structure allows it to be a versatile building block in the development of new drugs, particularly those targeting specific biological pathways or receptors.
In the synthesis of pharmaceuticals, 3-chloro-5-methoxyaniline can be further modified or combined with other chemical entities to create active pharmaceutical ingredients (APIs) with desired therapeutic properties. Its presence in the final drug product may contribute to the drug's efficacy, safety, and pharmacokinetic profile, making it an important component in the drug discovery and development process.

Check Digit Verification of cas no

The CAS Registry Mumber 10272-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10272-06:
(7*1)+(6*0)+(5*2)+(4*7)+(3*2)+(2*0)+(1*6)=57
57 % 10 = 7
So 10272-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8ClNO/c1-10-7-3-5(8)2-6(9)4-7/h2-4H,9H2,1H3

10272-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-5-Methoxyaniline

1.2 Other means of identification

Product number -
Other names 3-chloro-5-methoxyaniline

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:10272-06-7 SDS

10272-06-7Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 107, (2020/07/06)

Herein, compounds, compositions and methods for modulating inclusion formation and stress granules in cells related to the onset of neurodegenerative diseases, musculoskeletal diseases, cancer, ophthalmological diseases, and viral infections are described.

HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE

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Paragraph 0266-0267, (2019/05/15)

Provided are a heterocyclic carboxylic acid amide ligand and applications thereof in a copper catalyzed coupling reaction. Specifically, provided are uses of a compound represented by formula (I), definitions of radical groups being described in the specifications. The compound represented by formula (I) can be used as the ligand in the copper catalyzed coupling reaction of the aryl halogeno substitute, and is used or catalyzing the coupling reaction for forming the aryl halogeno substitute having C—N, C—O, C—S and other bonds.

Oxalic amide ligands, and uses thereof in copper-catalyzed coupling reaction of aryl halides

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Page/Page column 89-90, (2020/01/09)

The present invention provides oxalic amide ligands and uses thereof in copper-catalyzed coupling reaction of aryl halides. Specifically, the present invention provides a use of a compound represented by formula I, wherein definitions of each group are described in the specification. The compound represented by formula I can be used as a ligand in copper-catalyzed coupling reaction of aryl halides for the formation of C—N, C—O and C—S bonds.

SULPHONYL UREA DERIVATIVES AS NLRP3 INFLAMMASOME MODULATORS

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Paragraph 01089, (2019/07/13)

The present disclosure relates to compounds of Formula (I): (I) and to their pharmaceutically acceptable salts, pharmaceutical compositions, methods of use, and methods for their preparation. The compounds disclosed herein are useful for inhibiting the maturation of cytokines of the IL-1 family by inhibiting inflammasomes and may be used in the treatment of disorders in which inflammasome activity is implicated, such as inflammatory, autoinflammatory and autoimmune diseases and cancers.

QUINUCLIDINES FOR MODULATING ALPHA 7 ACTIVITY

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, (2016/02/29)

Provided are substituted quinuclidine compounds, pharmaceutical compositions comprising such compounds, and methods of modulating α7 nicotinic acetylcholine receptors and treating neurological disorders using such compounds.

Assembly of Primary (Hetero)Arylamines via CuI/Oxalic Diamide-Catalyzed Coupling of Aryl Chlorides and Ammonia

Fan, Mengyang,Zhou, Wei,Jiang, Yongwen,Ma, Dawei

supporting information, p. 5934 - 5937 (2015/12/11)

A general and practical catalytic system for aryl amination of aryl chlorides with aqueous or gaseous ammonia has been developed, with CuI as the catalyst and bisaryl oxalic diamides as the ligands. The reaction proceeds at 105-120°C to provide a diverse set of primary (hetero)aryl amines in high yields with various functional groups.

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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Page/Page column 94, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

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