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METHYL 2-AMINO-4,5-DIMETHYL-BENZOATE, also known as methyl 2-amino-4,5-dimethylbenzoate, is a chemical compound with the molecular formula C10H13NO2. It is a derivative of benzoic acid, featuring an amino group and two methyl groups attached to the benzene ring. METHYL 2-AMINO-4,5-DIMETHYL-BENZOATE is recognized for its unique structure and reactivity, making it a valuable intermediate in the synthesis of pharmaceuticals and organic compounds.

19258-73-2

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19258-73-2 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 2-AMINO-4,5-DIMETHYL-BENZOATE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, METHYL 2-AMINO-4,5-DIMETHYL-BENZOATE serves as a building block, facilitating the creation of a wide range of organic compounds due to its reactive functional groups.
Used in Agricultural Industry:
METHYL 2-AMINO-4,5-DIMETHYL-BENZOATE is utilized as a chemical intermediate in the development of agrochemicals, potentially contributing to the production of pesticides or other agricultural products that enhance crop protection and yield.
Used in Chemical Industry:
METHYL 2-AMINO-4,5-DIMETHYL-BENZOATE is also employed in the chemical industry for various applications, leveraging its structural and reactive attributes to produce a spectrum of chemical products for diverse uses.

Check Digit Verification of cas no

The CAS Registry Mumber 19258-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,5 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19258-73:
(7*1)+(6*9)+(5*2)+(4*5)+(3*8)+(2*7)+(1*3)=132
132 % 10 = 2
So 19258-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-6-4-8(10(12)13-3)9(11)5-7(6)2/h4-5H,11H2,1-3H3

19258-73-2SDS

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 2-amino-4,5-dimethylbenzoate

1.2 Other means of identification

Product number -
Other names methyl 4,5-dimethyl-2-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:19258-73-2 SDS

19258-73-2Downstream Products

19258-73-2Relevant academic research and scientific papers

NONMUSCLE MYOSIN II INHIBITORS FOR SUBSTANCE USE RELAPSE

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Page/Page column 73-74; 79-80, (2020/01/08)

The invention can provide compounds, analogs of blebbistatin, effective and selective inhibitors of nonmuscle myosin II relative to cardiac myosin II. Compounds can be used in the method of treating a disease, disorder, or medical condition in a patient, comprising modulating myosin II ATPase, such as treatment of substance abuse relapse disorder, or of renal disease, cancer and metastasis, benign prostate hyperplasia, hemostasis or thrombosis, nerve injury including retinal damage, lung fibrosis, liver fibrosis, arthrofibrosis, wound healing, spinal cord injury, periodontitis, glaucoma and immune-related diseases including multiple sclerosis; or wherein the disease, disorder, or medical condition comprises addiction including abuse of or addiction to anything classified as a Substance-Related or Addictive Disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM), such as, but not limited to, cocaine, opioids, amphetamines, ethanol, cannabis/marijuana, nicotine, and activities including gambling Compounds are of general formula (I) with substituents as defined herein.

N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors

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, (2008/06/13)

Described are compounds of formula (I), wherein W is O or S; X is NR8; Y is CR9R10-(CH2)n wherein R9 and R10 are independently of each other hydrogen or lower alkyl, and n is an integer of

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