3095-48-5

Basic information

• Product Name: 4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER
• Synonyms: 4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER;Methyl 4-aMino-3,5-diMethylbenzoate;Benzoic acid, 4-aMino-3,5-diMethyl-, Methyl ester
• CAS NO: 3095-48-5
• Molecular Formula: C₁₀H₁₃NO₂
• Molecular Weight: 179.21572
• Mol File: 3095-48-5.mol
• Article Data: 12

Chemical Properties

• Melting Point: 106-107℃
• Boiling Point: 331.341 °C at 760 mmHg
• Flash Point: 180.604 °C
• Appearance: /
• Density: 1.105 g/cm³
• Storage Temp.: 2-8°C(protect from light)
• PKA: 2.17±0.10(Predicted)
• CAS DataBase Reference: 4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(3095-48-5)
• EPA Substance Registry System: 4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(3095-48-5)

Safety Data

• Hazardous Substances Data: 3095-48-5(Hazardous Substances Data)

Usage

General Description

4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER, also known as methyl 4-amino-3,5-dimethylbenzoate, is a chemical compound with the molecular formula C10H13NO2. It is a methyl ester derivative of 4-amino-3,5-dimethylbenzoic acid and is commonly used in the synthesis of pharmaceuticals and organic compounds. 4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER is a white to off-white powder with a molecular weight of 179.22 g/mol and a melting point of around 118-120°C. It is typically used as an intermediate in the production of active pharmaceutical ingredients and organic compounds for various industrial uses. Additionally, it may be used as a reagent in chemical reactions and as a building block in organic synthesis.

Upstream product

• 569344-32-7 methyl 4-amino-3-methyl-5-methylthiomethylbenzoate 
• 18595-14-7 methyl 4-amino-3-methylbenzoate 
• 75-18-3 dimethylsulfide 
• 499-06-9 3,5-dimethylbenzoic acid 
• 79-37-8 oxalyl dichloride 
• 3277-04-1 3,5-dimethyl-4-nitro-benzoic acid methyl ester 
• 67-56-1 methanol 
• 4919-40-8 4-amino-3,5-dimethylbenzoic acid 
• 3095-38-3 3,5-dimethyl-4-nitrobenzoic acid 

Downstream Products

• 56066-81-0 4'-amino-3',5'-dimethyl-2-(methylsulfonyl)-acetophenone 
• 56066-87-6 4'-(dimethylamino)-3',5'-dimethyl-2-(methylsulfonyl)-acetophenone 
• 948552-50-9 3,5-dimethyl-4-propionylamino-benzoic acid methyl ester 
• 167626-74-6 3,5-dimethyl-4-propionylaminobenzoic acid 
• 167626-17-7 1-(3,5-dimethyl-4-propionylamino)benzoyl-4-(N-methyl-2-phenylethyl)aminopiperidine 
• 56066-86-5 4-(dimethylamino)-3,5-dimethyl-benzoic acid methyl ester 
• 432022-88-3 4-bromo-3,5-dimethylbenzoic acid methyl ester 
• 184041-97-2 N-(4-chloro-3-methyl-5-isoxazolyl)-N-(methoxyethoxymethyl) 2-(4-methoxycarbonyl-2,6-dimethyl)phenylaminocarbonyl-3-thiophenesulfonamide 
• 1529760-72-2 methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate 
• 87-62-7 2,6-dimethylaniline 
• 1616605-04-9 C₁₇H₁₉NO₅S 
• 56066-88-7 4-(dimethylamino)-3,5-dimethyl-α-[(methylsulfonyl)-methyl]-benzyl alcohol 
• 56066-82-1 4-amino-3,5-dimethyl-α-[(methylsulfonyl)-methyl]-benzyl alcohol 
• 87725-33-5 4-dimethylamino-3,5-dimethyl-benzoic acid 

Relevant articles and documents

Photoinduced properties of methyl ester of 2,6-dimethyl-1-amino-4-benzoic acid: Evidence of charge transfer emission from a weak primary amino donor

Photophysical properties of methyl ester of 2,6-dimethyl-1-amino-4-benzoic acid (M26DMB) have been investigated using steady state absorption and emission spectroscopy and time-resolved emission spectroscopy. Interestingly, not only in polar solvents, the molecule M26DMB having a weak primary amino donor group shows broad red-shifted emission band even in non-polar environment which in all probability arises from closely spaced local and charge transfer (CT) states. Clear dual fluorescence in polar protic solvents comprises of less intense local emission band and strong red-shifted CT band. The position of the red-shifted emission band is dependent on both the polarity and the hydrogen-bonding ability of the solvent.

Discovery of substituted-2,4-dimethyl-(naphthalene-4-carbonyl)amino-benzoic acid as potent and selective EP4 antagonists

A novel series of EP4 antagonists, based on a quinoline scaffold, has been discovered. Medicinal chemistry efforts to optimize the potency of the initial hit are described. A highly potent compound in a clinically relevant human whole blood assay was iden

DIMETHYL-BENZOIC ACID COMPOUNDS

The present invention provides a compound of the Formula II: wherein A is: * R 1 is CH3, CF 3, or F; * R 2 is H, CH3, or F; * R 3 is CH3, OCH 3, OH, F; R 4 is OH or CH 20H; and *