Methyl 3-amino-4-methylbenzoate

Methyl 3-amino-4-methylbenzoate Structure
CAS No.
18595-18-1
Chemical Name:
Methyl 3-amino-4-methylbenzoate
Synonyms
AKOS BB-3092;3-Amino-p-toluic;Compound Fr13901;Methyl 3-amino-4-met;Nilotinib Impurity 25;LABOTEST-BB LT00848257;Nilotinib EP Impurity B;3-Amino-4-Methylbenzoate;METHYL 3-AMINO-P-TOLUATE;3-amino-2,4-dimethylbenzoate
CBNumber:
CB4316035
Molecular Formula:
C9H11NO2
Molecular Weight:
165.19
MOL File:
18595-18-1.mol
MSDS File:
SDS
Modify Date:
2024/3/28 13:36:31

Methyl 3-amino-4-methylbenzoate Properties

Melting point 113-117 °C(lit.)
Boiling point 296.3±20.0 °C(Predicted)
Density 1.132±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly), Methanol (Slightly)
pka 3.31±0.10(Predicted)
form Crystalline Powder
color White to cream
BRN 2088611
InChIKey YEPWCJHMSVABPQ-UHFFFAOYSA-N
LogP 1.7 at 22℃ and pH7
CAS DataBase Reference 18595-18-1(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280-P280-P302+P352-P304+P340+P312-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37
WGK Germany  3
Hazard Note  Irritant
HS Code  29224999
NFPA 704
1
2 0

Methyl 3-amino-4-methylbenzoate price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ALFA India ALF-A15348-22 Methyl 3-amino-4-methylbenzoate, 97% 18595-18-1 100g ₹32982 2022-05-26 Buy
ALFA India ALF-A15348-14 Methyl 3-amino-4-methylbenzoate, 97% 18595-18-1 25g ₹3388 2022-05-26 Buy
TCI Chemicals (India) A1432 Methyl 3-Amino-4-methylbenzoate min. 98.0 % 18595-18-1 25G ₹4700 2022-05-26 Buy
ALFA India ALF-A15348-06 Methyl 3-amino-4-methylbenzoate, 97% 18595-18-1 5g ₹1230 2022-05-26 Buy
Product number Packaging Price Buy
ALF-A15348-22 100g ₹32982 Buy
ALF-A15348-14 25g ₹3388 Buy
A1432 25G ₹4700 Buy
ALF-A15348-06 5g ₹1230 Buy

Methyl 3-amino-4-methylbenzoate Chemical Properties,Uses,Production

Description

Methyl 3-amino-4-methylbenzoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Chemical Properties

Beige powder

Uses

Methyl 3-Amino-4-methylbenzoate is used as a reagent in the synthesis of perfluoroalkylated indoles which are very useful in drug development. It was also used in the preparation of 4-(pyrimidin-2-ylamino) benzamide derivatives which are designed as inhibitors of hedgehog signalling pathway (target of cancer treatment).

Application

Methyl 3-amino-4-methylbenzoate can be used for:
To prepare the methyl 4-methyl-3-((4-(proparg-1-yloxy)benzyl)amino)benzoate, 4-proparg-1-yloxybenzaldehyde (16) and methyl 3-amino-4-methylbenzoate were reacted according to the method IA.
Synthesis of Methyl 4-methyl-3-((4-(2-methylthiazol-4-yl)benzoyl)amino)benzoate
Synthesis of 4-Methyl-3-((4-(2-methylthiazol-4-yl)benzoyl)amino)benzamide
Synthesis of methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1 (2H)-yl)-4-methylbenzoate
Synthesis of methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1 (2H)-yl)-4-methylbenzoate
Synthesis of (5-Carbomethoxy-2-methylphenyl)(4-hydroxypheny)diazene: To a solution of 6N HC1 (6 mL) was added methyl 3-amino-4-methylbenzoate (1.62 g, 10.0 mmol). The solution was cooled in an ice-bath, and was diazotized by adding sodium nitrite (0.9 g, 12.0 mmol). To a cold solution of phenol in 21% aqueous NaOH solution (6 mL) was added diazotized solution slowly. After 20 min, the solution was acidfied by adding 4 N aqueous HC1 and was poured into the cold water, filtered, and washed with water. Recrystallization from ethanol gave the product (2.0 g, 74%) as red crystals, mp 181.3-182.2 °C.

Preparation

Synthesis of Methyl 3-amino-4-methylbenzoate: Nitro ester Methyl 4-methyl-3-nitrobenzoate (80 g, 0.410 mol) was subjected to hydrogenation in a Parr shaker in MeOH using Raney Ni as the catalyst (5 g, 20 mol %) at 50 psi for 8 hours. The catalyst was filtered off, washed thoroughly with MeOH and the combined filtrates concentrated under reduced pressure to furnish a yellow solid (65.0 g). Yield : 96% Mp : 114-5°C (lit.14 Mp 116°C)

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METHYL 3-AMINO-4-METHYLBENZOATE METHYL 3-AMINO-P-TOLUATE LABOTEST-BB LT00848257 3-Amino-p-Toluic Acid Methyl Ester 3-Amino-4-Methyl Benzoic Acid Methyl Ester 3-Amino-4-Methylbenzoate 3-Amino-p-toluic Methyl 3-amino-4-methylbenzoate 98% Methyl 3-Amion-4-Methylbenzoate AKOS BB-3092 3-AMINO-4-METHYLBENZOIC ACID METHYL ESTER 3-AMINO-P-TOLUIC ACID METHYL ESTER Methyl4-Methyl-3-Aminobenzoate Methyl 3-amino-4-met 3-Amino-4-methylbenzoic Acid Methyl Ester Methyl 3-Amino-p-toluate 3-Amino-p-toluic Acid Methyl Ester Methyle3-amino-4-methylbenzoate 5-(Methoxycarbonyl)-2-methylaniline, 2-Amino-4-(methoxycarbonyl)toluene, 5-(Methoxycarbonyl)-o-toluidine Benzoic acid, 3-aMino-4-Methyl-, Methyl ester Methyl-3-amino-4-methylbenozate 3-amino-2,4-dimethylbenzoate Nilotinib Impurity 25 Nilotinib EP Impurity B Methyl 3-Amino-4-methylbenzoate > Methyl 3-amino-4-methylbenzoate 18595-18-1 Nilotinib USP Related Compound B Benzoic acid, 3-amino-4-methyl-, methyl ester (9CI, ACI) 3-amino-4-methyl-Benzoic acid methyl ester (9CI ACI) Compound Fr13901 Nilotinib Hydrochloride Monohydrate EP Impurity B Nilotinib Impurity 17(Nilotinib EP Impurity B) 18595-18-1 18585-18-1 Esters Organic Building Blocks Building Blocks Carbonyl Compounds C8 to C9 Building Blocks C8 to C9 Carbonyl Compounds Chemical Synthesis Organic Building Blocks Aromatic Esters Esters Phenyls & Phenyl-Het FINE Chemical & INTERMEDIATES Acids and Derivatives Amines and Anilines bc0001