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202146-16-5

METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE, with the molecular formula C9H10ClNO2, is a chemical compound belonging to the aromatic benzoate class. It serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, and is valued for its role as a building block in organic synthesis, contributing to the preparation of medicinally relevant molecules.

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  • 202146-16-5 Structure

  • Basic information

    1. Product Name: METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE
    2. Synonyms: METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE;4-Amino-3-chloro-5-methylbenzoic acid methyl ester
    3. CAS NO:202146-16-5
    4. Molecular Formula: C9H10ClNO2
    5. Molecular Weight: 199.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 202146-16-5.mol

  • Chemical Properties

    1. Melting Point: 80-82
    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: METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE(202146-16-5)
    11. EPA Substance Registry System: METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE(202146-16-5)

  • Safety Data

    1. Hazard Codes: Xi
    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: 202146-16-5(Hazardous Substances Data)

202146-16-5 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE is used as a synthetic intermediate for the development of various pharmaceuticals, leveraging its chemical structure to create compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE is utilized as a precursor in the synthesis of agrochemicals, contributing to the development of products designed to enhance crop protection and yield.
Used as a Building Block in Organic Synthesis:
METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE is employed as a fundamental building block in organic synthesis, enabling the creation of a wide array of chemical compounds for diverse applications across various industries.
It is crucial to handle METHYL 4-AMINO-3-CHLORO-5-METHYLBENZOATE with caution due to its potential health risks if not used properly, emphasizing the importance of safety measures in its application and manipulation.

Check Digit Verification of cas no

The CAS Registry Mumber 202146-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,1,4 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 202146-16:
(8*2)+(7*0)+(6*2)+(5*1)+(4*4)+(3*6)+(2*1)+(1*6)=75
75 % 10 = 5
So 202146-16-5 is a valid CAS Registry Number.

202146-16-5SDS

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 methyl 4-amino-3-chloro-5-methylbenzoate

1.2 Other means of identification

Product number -
Other names methyl 4-amino-5-chloro-3-methylbenzoate

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:202146-16-5 SDS

202146-16-5Relevant articles and documents

PREPARATION AND APPLICATION OF CLASS OF N-CONTAINING HETEROCYCLIC COMPOUNDS HAVING IMMUNOREGULATORY FUNCTION

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Paragraph 0093-0095, (2021/06/10)

The present invention discloses the preparation and application of heterocyclic compound having immunoregulatory function. Specifically, the present invention discloses a compound having a structure according to Formula I, wherein the definition of each g

Novel selective hindlimb vasodilators: Synthesis and biological activity of 1-acyl-4-aminopiperidine derivatives

Teramoto, Shuji,Tanaka, Michinori,Shimizu, Hiroshi,Fujioka, Takafumi,Tabusa, Fujio,Imaizumi, Takashi,Yoshida, Kenji,Fujiki, Hiroyuki,Mori, Toyoki,Sumida, Takumi,Tominaga, Michiaki

, p. 3033 - 3044 (2007/10/03)

A series of 6-(4-amino-1-piperidinyl)carbonyl-2(1H)-quinolinones, and their open form derivatives, were synthesized and evaluated for their ability to stimulate femoral artery blood flow (FBF) in the canine hindlimb. All members of this series stimulated

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