122744-78-9

Basic information

• Product Name: 2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID
• Synonyms: 2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID;BOC-2-AMINO-4,5-DIMETHOXYBENZOIC ACID;ANTHRANILIC ACID, N-BOC-4,5-DIMETHOXY;N-BOC-4,5-DIMETHOXYANTHRANILIC ACID;2-[[(1,1-Dimethylethoxy)carbonyl]amino]-4,5-dimethoxybenzoic acid
• CAS NO: 122744-78-9
• Molecular Formula: C₁₄H₁₉NO₆
• Molecular Weight: 297.3
• Mol File: 122744-78-9.mol

Chemical Properties

• Boiling Point: 378.4°Cat760mmHg
• Flash Point: 182.6°C
• Appearance: /
• Density: 1.244g/cm³
• Vapor Pressure: 2.12E-06mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: 2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID(122744-78-9)
• EPA Substance Registry System: 2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID(122744-78-9)

Safety Data

• Safety Statements: 24/25
• HazardClass: IRRITANT
• Hazardous Substances Data: 122744-78-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID is used as a building block in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications, such as treating diseases or managing symptoms.
Used in Agrochemical Industry:
In the agrochemical industry, 2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID is used as a precursor in the production of agrochemicals, including pesticides and herbicides. Its chemical properties enable the creation of effective compounds that can protect crops from pests and enhance agricultural productivity.
Used in Organic Synthesis:
2-TERT-BUTOXYCARBONYLAMINO-4,5-DIMETHOXY-BENZOIC ACID is used as a versatile intermediate in organic synthesis. Its presence in various chemical reactions allows for the formation of a wide range of compounds with diverse applications in different industries, such as the synthesis of dyes, polymers, and other specialty chemicals.

InChI:InChI=1/C14H19NO6/c1-14(2,3)21-13(18)15-9-7-11(20-5)10(19-4)6-8(9)12(16)17/h6-7H,1-5H3,(H,15,18)(H,16,17)

Upstream product

• 124-38-9 carbon dioxide 
• 102421-43-2 N-((1,1-dimethylethyl)oxycarbonyl)-3,4-dimethoxyaniline 
• 24424-99-5 di-tert-butyl dicarbonate 
• 5653-40-7 2-Amino-4,5-dimethoxybenzoic acid 

Downstream Products

• 733810-04-3 [4,5-dimethoxy-2-(3-chloro-4-fluorophenylcarbamoyl)-phenyl]-carbamic acid tert-butyl ester 
• 733810-00-9 [4,5-dimethoxy-2-(3-methoxy-phenylcarbamoyl)-phenyl]-carbamic acid tert-butyl ester 
• 733809-93-3 [4,5-dimethoxy-2-(3-trifluoromethyl-phenylcarbamoyl)-phenyl]-carbamic acid tert-butyl ester 
• 733809-74-0 [4,5-dimethoxy-2-cyclohexylcarbamoylphenyl]-carbamic acid tert-butyl ester 
• 733809-81-9 [4,5-dimethoxy-2-(1-phenyl-ethylcarbamoyl)-phenyl]-carbamic acid tert-butyl ester 
• 733809-87-5 [4,5-dimethoxy-2-(3-bromophenylcarbamoyl)-phenyl]-carbamic acid tert-butyl ester 
• 1221573-83-6 C₄₂H₃₈F₁₇N₃O₁₄S 
• 1221571-92-1 C₄₀H₄₄F₁₇N₃O₉S 
• 1221572-07-1 C₄₁H₄₆F₁₇N₃O₁₀S 
• 1221571-95-4 C₄₃H₄₂F₁₇N₃O₉S 
• 1221572-11-7 C₄₄H₄₄F₁₇N₃O₁₀S 
• 1221574-08-8 C₄₀H₄₂F₁₇N₃O₁₂S 
• 1198473-11-8 C₁₆H₂₄N₂O₆ 
• 408509-80-8 4,5-dimethoxy-N,2-dimethylaniline 

Relevant articles and documents

Facile synthesis and antitumor activity of novel N(9) methylated AHMA analogs

A facile synthesis of novel antitumor N(9)-methyl-3-(9-acridinylamino)-5- hydroxymethylaniline (AHMA) derivatives is described. Boc protection of aminobenzoic acids followed by LiAlH4 reduction yielded novel methylaminobenzyl alcohol reactants. Their interaction with 9-chloroacridine provides N(9)-methylated AHMA derivatives for biological screening. A preliminary anti-proliferative assay against seven cancer cell lines identified compounds with low μM IC50 values. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

Synthesis of a quinolone library from ynones

A library of 72 quinolones was synthesized from substituted anthranilic acids, using ynone intermediates. These masked β-dicarbonyl synthons allowed cyclization under milder conditions than previously reported quinolone syntheses.

Benzamides and benzamidines as specific inhibitors of epidermal growth factor receptor and v-Src protein tyrosine kinases

The benzamides 1 and the benzamidines 2 as well as the cyclic benzamidines 3 were designed and synthesized as the mimics of 4-anilinoquinazolines for an inhibitor of EGFR tyrosine kinase. The specific inhibitions of EGFR tyrosine kinase were observed in the benzamides 1c and 1d, and the benzamidine 2a, whereas the specific inhibitions of v-Src kinase were observed in the benzamide 1j and the benzamidine 2d at a 10μg/mL concentration of compounds. The cyclic benzamidines 3a and 3b showed potent kinase inhibition of EGFR at a 1.0μg/mL concentration. According to the docking simulation using the X-ray structure of EGFR kinase domain in complex with erlotinib, the LigScore2 scoring function value of erlotinib was calculated as 5.61, whereas that of the benzamide 1c was 5.05. In a similar manner, the LigScore2 value of the cyclic benzamidine 3a was calculated as 5.10.

Synthesis and biological evaluation of benzamides and benzamidines: Structural requirement of a pyrimidine ring for inhibition of EGFR tyrosine kinase

The benzamides 1 and the benzamidines 2-3 were synthesized as the mimics of 4-anilinoquinazolines, which possess inhibition of epidermal growth factor receptor (EGFR) tyrosine kinase, and tested for cytotoxicity toward A431 and inhibitory activity toward

Secondary β-Aminobenzamide and Heteroatom Directed Lithiation in the Synthesis of 5,6-Dimethoxyanthanilamides and Related Compounds

Directed ortho-lithiation strategies have been applied in the synthesis of the dopamine D-2 antagonist (S)-6-amino-5-bromo-2,3-dimethoxy-N-benzamide (NCQ 318).The secondary β-amino side chain was found to be a powerful orth