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Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate is a versatile chemical compound with the molecular formula C9H10ClNO3. It is a derivative of benzenecarboxylate, featuring a methyl, amino, chloro, and methoxy group attached to the benzene ring. Known for its potential as a building block in organic chemistry, its diverse reactivity makes it a valuable component in the synthesis of various chemical products.

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  • 63603-10-1 Structure
  • Basic information

    1. Product Name: Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate
    2. Synonyms: Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate;Methyl 2-(benzyloxy)-5-methoxy-3-nitrobenzenecarboxylate;Methyl 3-amino-4-chloro-5-methoxybenzoate 95+%;2-Chloro-3-methoxy-5-(methoxycarbonyl)aniline;2-Chloro-3-methoxy-5-(methoxycarbonyl)aniline, 3-Amino-2-chloro-5-(methoxycarbonyl)anisole;methyl 3-amino-4-chloro-5-methoxybenzoate;3-Amino-4-chloro-5-methoxy-benzoic acid methyl ester
    3. CAS NO:63603-10-1
    4. Molecular Formula: C9H10ClNO3
    5. Molecular Weight: 216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63603-10-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 341.6±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.302±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.09±0.10(Predicted)
    10. CAS DataBase Reference: Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate(63603-10-1)
    12. EPA Substance Registry System: Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate(63603-10-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 63603-10-1(Hazardous Substances Data)

63603-10-1 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate serves as an intermediate for the production of agrochemicals. Its properties allow for the creation of compounds that can be used in pest control and crop protection.
Used in Dye and Pigment Production:
Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate is utilized in the production of dyes and pigments due to its chemical structure that can impart color to various materials. This makes it a valuable component in the manufacturing of colored products for different industries.
Used as a Building Block in Organic Chemistry:
Recognized for its potential as a building block in organic chemistry, Methyl 3-amino-4-chloro-5-methoxybenzenecarboxylate is employed in the creation of a wide range of chemical products. Its versatile reactivity allows for the synthesis of new compounds with diverse applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 63603-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,0 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63603-10:
(7*6)+(6*3)+(5*6)+(4*0)+(3*3)+(2*1)+(1*0)=101
101 % 10 = 1
So 63603-10-1 is a valid CAS Registry Number.

63603-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-amino-4-chloro-5-methoxybenzoate

1.2 Other means of identification

Product number -
Other names methyl 4-chloro-3-methoxy-5-aminobenzoate

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:63603-10-1 SDS

63603-10-1Relevant articles and documents

MACROCYCLIC DIAMINE DERIVATIVES AS ENT INHIBITORS FOR THE TREATMENT OF CANCERS, AND COMBINATION THEREOF WITH ADENOSINE RECEPTOR ANTAGONISTS

-

Paragraph 0486; 0554, (2021/10/15)

The present invention relates to macrocyclic diamine derivatives of formula II, including pharmaceutically acceptable salts and solvates thereof. Compounds of the invention are inhibitors of ENT family transporter, especially of ENT1, and are useful as therapeutic compounds for the treatment of cancers. The invention also relates to the combined use of the macrocyclic diamine derivatives with an adenosine receptor antagonist, for the treatment of cancers.

FUSED PYRIMIDINOPIPERIDINE DERIVATIVE, AND MANUFACTURING METHOD AND APPLICATION THEREOF

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, (2019/04/25)

The present invention relates to the fused pyrimidine piperidine cyclic derivative represented by the following formula (I) and a pharmaceutically acceptable salt thereof and a process for preparing the same, wherein R1, R2, R3

Therapeutic Aryl-Amido-Aryl Compounds and Their Use

-

, (2012/06/18)

The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain aryl-amido-aryl compounds of the following formula (for convenience, collectively referred to herein as “AAA compounds”), which, inter alia, a

THERAPEUTIC ARYL-AM I DO-ARYL COMPOUNDS AND THEIR USE

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, (2011/04/14)

The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain aryl-amido-aryl compounds of the following formula (for convenience, collectively referred to herein as "AAA compounds"), which, inter alia, a

Formal total synthesis of N-methylmaysenine

Wang, Lin,Gong, Jianxian,Deng, Lujiang,Xiang, Zheng,Chen, Zhixing,Wang, Yuefan,Chen, Jiahua,Yang, Zhen

supporting information; experimental part, p. 1809 - 1812 (2009/09/06)

A novel synthetic approach for the formal total synthesis of N-methylmaysenine (1) has been developed. Key steps Involve the Ti-mediated vlnylogous Mukaiyama aldol reaction of chlral ketene silyl N,O-acetal with β-dithiane-substituted aldehyde, an aldol c

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