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METHYL 3-AMINO-5-METHYLBENZOATE, with the chemical formula C9H11NO2, is a derivative of benzoic acid that features an amino and a methyl group. METHYL 3-AMINO-5-METHYLBENZOATE is recognized for its utility in various chemical and pharmaceutical applications, including its mild anesthetic properties that make it suitable for use in topical pain relief formulations.

18595-15-8

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18595-15-8 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 3-AMINO-5-METHYLBENZOATE is used as a chemical intermediate for the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used in Dyes and Pigments Production:
METHYL 3-AMINO-5-METHYLBENZOATE is used as a component in the production of dyes and pigments, adding to the color spectrum used in different industries.
Used in Topical Pain Relief Formulations:
METHYL 3-AMINO-5-METHYLBENZOATE is used as a mild anesthetic agent in topical formulations to provide pain relief, particularly for minor skin irritations and injuries.
Safety Considerations:
It is important to handle METHYL 3-AMINO-5-METHYLBENZOATE with care due to its potential harmful effects if ingested or inhaled, and its ability to cause skin and eye irritation. Proper safety measures should be taken during its use and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 18595-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,9 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18595-15:
(7*1)+(6*8)+(5*5)+(4*9)+(3*5)+(2*1)+(1*5)=138
138 % 10 = 8
So 18595-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-6-3-7(9(11)12-2)5-8(10)4-6/h3-5H,10H2,1-2H3

18595-15-8 Well-known Company Product Price

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  • Aldrich

  • (JWP00113)  3-Amino-5-methyl-benzoic acid methyl ester  AldrichCPR

  • 18595-15-8

  • JWP00113-1G

  • 3,866.85CNY

  • Detail

18595-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-amino-5-methylbenzoate

1.2 Other means of identification

Product number -
Other names 3-amino-5-methyl-benzoic acid methyl ester

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:18595-15-8 SDS

18595-15-8Downstream Products

18595-15-8Relevant academic research and scientific papers

FUSED BICYCLIC COMPOUNDS AND USES THEREOF IN MEDICINE

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Paragraph 00196; 00261, (2019/03/05)

Fused bicyclic compounds and uses thereof in medicine. In particular, provided are fused bicyclic compounds used as ASK1 active regulator and and use of the compounds in the manufacture of a drug for treating a disease regulated by ASK1. Further provided are a pharmaceutical composition and a method of treating a disease regulated by ASK1 comprising administering the compounds or pharmaceutical composition thereof.

PROTEIN KINASE INHIBITORS FOR PROMOTING LIVER REGENERATION OR REDUCING OR PREVENTING HEPATOCYTE DEATH

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Page/Page column 32; 48, (2018/08/12)

The invention relates to MKK4 (mitogen-activated protein kinase 4) and their use in promoting liver regeneration or reducing or preventing hepatocyte death. The MKK4 inhibitors selectively inhibit protein kinase MKK4 over protein kinases JNK and MKK7.

1, 3, 4-BENZOTRIAZEPIN-2-ONE SALTS AND THEIR USE AS CCK RECEPTOR LIGANDS

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Page 71-72, (2008/06/13)

This invention relates to pharmaceutically acceptable salts of compounds of formula (I) wherein: W is N or N+-O-; R2 is an optionally substituted C1 to C18 hydrocarbyl group wherein up to three C atoms may optionally be replaced by N, O and/or S atoms. R3 is -(CR11R12)m-X-(CR13R14)p-R9; m is 0, 1, 2, 3 or 4; p is 0, 1 or 2; X is a bond, -CR15=CR16-, -C≡C-, C(O)NH, NHC(O), C(O)NMe, NMeC(O), C(O)O, NHC(O)NH, NHC(O)O, OC(O)NH, NH, O, CO, SO2, SO2NH, C(O)NHNH, R9 is H ; C1 to C6 alkyl ; or phenyl, naphthyl, pyridyl, benzimidazolyl, indazolyl, quinolinyl, isoquinolinyl, tetrahydroisoquinolinyl, indolinyl, isoindolinyl, indolyl, isoindolyl or 2-pyridonyl substituted with -L-Q. R4 is an optionally substituted C1 to C18 hydrocarbyl group wherein up to three C atoms may optionally be replaced by N, O and/or S atoms ; and Such salts are useful, for example, for the treatment of gastrin related disorders.

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