36052-26-3

Basic information

• Product Name: 6-AMINOPICOLINIC ACID METHYL ESTER
• Synonyms: 6-AMINOPICOLINIC ACID METHYL ESTER;2-PYRIDINECARBOXYLIC ACID, 6-AMINO-,METHYL ESTER;Methyl 6-aminopicolinate;Methyl 6-aminopyridine-2-carboxylate 98%;2-Pyridinecarboxylicacid,6-amino-,methylester(9CI);Methyl 2-amino-6-pyridinecarboxylate;methyl 6-amino-2-pyridinecarboxylate;Methyl 6-aminopyridine-2-carboxylate
• CAS NO: 36052-26-3
• Molecular Formula: C₇H₈N₂O₂
• Molecular Weight: 152.15
• EINECS: 615-805-8
• Product Categories: GLYCINESCAFFOLD;Amines;blocks;Carboxes;Pyridines;pharmacetical
• Mol File: 36052-26-3.mol
• Article Data: 27

Chemical Properties

• Melting Point: 95.0 to 99.0 °C
• Boiling Point: 321.1 °C at 760 mmHg
• Flash Point: 148 °C
• Appearance: /
• Density: 1.238 g/cm³
• Vapor Pressure: 0.000305mmHg at 25°C
• Refractive Index: 1.57
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 1.83±0.10(Predicted)
• CAS DataBase Reference: 6-AMINOPICOLINIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINOPICOLINIC ACID METHYL ESTER(36052-26-3)
• EPA Substance Registry System: 6-AMINOPICOLINIC ACID METHYL ESTER(36052-26-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 36052-26-3(Hazardous Substances Data)

Usage

Chemical Properties

White to off-white powder

InChI:InChI=1/C7H8N2O2/c1-11-7(10)5-3-2-4-6(8)9-5/h2-4H,1H3,(H2,8,9)

Upstream product

• 26893-72-1 6-acetamido-picolinic acid 
• 88061-85-2 methyl 3-nitroimidazo<1,2-a>pyridine-5-carboxylate 
• 67-56-1 methanol 
• 824-40-8 2-pyridinecarboxylic acid N-oxide 
• 38195-81-2 1-oxy-pyridine-2-carboxylic acid methyl ester 
• 1824-81-3 2-Amino-6-methylpyridine 
• 5327-33-3 2-acetylamino-6-methylpyridine 
• 88047-55-6 methyl imidazo<1,2-a>pyridine-5-carboxylate 
• 23628-31-1 6-aminopicolinic acid 
• 118267-40-6 C₁₁H₁₄N₂O₃ 
• 5453-67-8 2,6-bis(methoxycarbonyl)pyridine 
• 1262043-88-8 methyl 6-(benzyloxycarbonylamino)-pyridine-2-carboxylate 
• 499-83-2 Pyridine-2,6-dicarboxylic acid 
• 7170-36-7 6-(methoxycarbonyl)pyridine-2-carboxylic acid 

Downstream Products

• 98953-28-7 6-acetylamino-pyridine-2-carboxylic acid methyl ester 
• 13538-41-5 6-aminopyridine-2-carboxamide 
• 178876-83-0 methyl 6-amino-3-bromo-pyridine-2-carboxylate 
• 178876-82-9 6-amino-5-bromo-pyridine-2-carboxylic acid methyl ester 
• 774213-93-3 methyl 1-(2-tert-butoxy-2-oxoethyl)-3-cyclohexyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate 
• 774213-92-2 methyl 2-bromo-1-(2-tert-butoxy-2-oxoethyl)-3-cyclohexyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate 
• 774213-95-5 [3-cyclohexyl-6-(methoxycarbonyl)-2-phenyl-1H-pyrrolo[2,3-b]pyridin-1-yl]acetic acid 
• 774213-96-6 methyl 3-cyclohexyl-1-[2-(dimethylamino)-2-oxoethyl]-2-phenyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate 
• 774213-94-4 methyl 1-(2-tert-butoxy-2-oxoethyl)-3-cyclohexyl-2-phenyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate 
• 178876-86-3 methyl 5-bromo-6-oxo-1,6-dihydropyridine-2-carboxylate 
• 178876-84-1 6-Acetylamino-5-bromo-pyridine-2-carboxylic acid methyl ester 
• 111753-15-2 methyl 3-aminoimidazo<1,2-a>pyridine-5-carboxylate 
• 88061-85-2 methyl 3-nitroimidazo<1,2-a>pyridine-5-carboxylate 
• 79651-64-2 (6-Amino-pyridin-2-yl)-methanol 

Relevant articles and documents

POLY HETEROCYCLIC CONJUGATES AND THEIR PHARMACEUTICAL USES

Compounds of Formula (I) shown below and a pharmaceutical composition containing one of the compounds: Each of the variables is defined herein. Also disclosed is a method of treating a condition associated with uncontrolled cell growth with a compound of Formula (I).

Discovery of highly reactive peptide tag by ELISA-type screening for specific cysteine conjugation

We report the discovery of a highly reactive peptide tag for the specific cysteine conjugation of proteins. Screening of cysteine-containing peptides using ELISA-type screening yielded a 19-amino acid tag (DCPPPDDAADDAADDAADD), named DCP3 tag, which enabl

Cation-halide transport through peptide pores containing aminopicolinic acid

Synthetic pores that selectively transport ions of biological significance through membranes could be potentially used in medical diagnostics or therapeutics. Herein, we report cation-selective octapeptide pores derived from alanine and aminopicolinic acid. The ion transport mechanism through the pores has been established to be a cation-chloride symport. The cation-chloride co-transport is biologically essential for the efficient functioning of the central nervous system and has been implicated in diseases such as epilepsy. The pores formed in synthetic lipid bilayers do not exhibit any closing events. The ease of synthesis as well as infinite lifetimes of these pores provides scope for modifying their transport behaviour to develop sensors.