Methyl 3-aMino-4-((tert-butoxycarbonyl)aMino)benzoate

Methyl 3-aMino-4-((tert-butoxycarbonyl)aMino)benzoate - Names and Identifiers

Name	3-amino-4-tert-butoxycarbonylamino-benzoic acid methyl ester
Synonyms	Methyl 3-aMino-4-((tert-butoxycarbonyl)aMino)benzoate 3-AMINO-4-TERT-BUTOXYCARBONYLAMINO-BENZOIC ACID METHYL ESTER 3-amino-4-tert-butoxycarbonylamino-benzoic acid methyl ester 2- AMino-4-tert-butoxycarbonylaMino-benzoic acid Methyl ester Methyl 3-amino-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)benzoate 3-Amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]benzoic acid methyl ester Benzoic acid, 3-amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester
CAS	327046-67-3
InChI	InChI=1S/C13H18N2O4/c1-13(2,3)19-12(17)15-10-6-5-8(7-9(10)14)11(16)18-4/h5-7H,14H2,1-4H3,(H,15,17)

Methyl 3-aMino-4-((tert-butoxycarbonyl)aMino)benzoate - Physico-chemical Properties

Molecular Formula	C13H18N2O4
Molar Mass	266.29
Storage Condition	2-8°C

Methyl 3-aMino-4-((tert-butoxycarbonyl)aMino)benzoate - Introduction

acid methyl ester is an organic compound with the molecular formula C15H20N2O4, which is a solid crystal and soluble in organic solvents such as ethanol and dimethyl sulfoxide.

Its main properties are as follows:
-Appearance: White crystalline solid
-Melting point: 114-115 ° C
-Melting point: 122-124 ° C
-Molecular weight: 300.33g/mol

acid methyl ester has important applications in drug synthesis and biochemical research.

According to its structural characteristics, it can be used as raw materials and reagents in the following aspects:
-as a drug intermediate: acid methyl ester can be used to synthesize certain drugs, such as drugs, antibiotics and tumor treatment drugs.
-Biochemical research: It can be applied to the modification of proteins and peptides, as well as other biochemical experiments.

The preparation method of acid methyl ester usually includes the following steps:
1. First, benzoic acid is reacted with hydrogen peroxide in an organic solvent to generate peroxybenzoic acid.
2. Next, benzoic acid peroxide is reacted with dimethylethanolamine under alkaline conditions to form formyl amine.
3. Finally, the formyl amine is reacted with trimethylsilyl aluminum hydride under the protection of inert gas to generate acid methyl ester.

Regarding safety information, the relevant information of acid methyl ester may be limited. Please read the product manual carefully before use and use it in accordance with the operating instructions. In addition, follow appropriate laboratory safety practices and use the necessary personal protective equipment.

Last Update：2024-04-09 21:01:54