853058-07-8

Basic information

• Product Name: CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-,PHENYLMETHYL ESTER
• Synonyms: CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-,PHENYLMETHYL ESTER;N-(6-Amino-2-pyridinyl)-carbamic acid phenylmethyl ester;benzyl (6-aminopyridin-2-yl)carbamate
• CAS NO: 853058-07-8
• Molecular Formula: C₁₃H₁₃N₃O₂
• Molecular Weight: 243.265
• Mol File: 853058-07-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-,PHENYLMETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-,PHENYLMETHYL ESTER(853058-07-8)
• EPA Substance Registry System: CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-,PHENYLMETHYL ESTER(853058-07-8)

Safety Data

• Hazardous Substances Data: 853058-07-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-, PHENYLMETHYL ESTER is used as a building block for the synthesis of various drugs and pharmaceuticals. Its unique structure and functional groups make it a valuable component in the development of new medications.
Used in Agricultural Chemistry:
CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-, PHENYLMETHYL ESTER may have potential applications in the field of agricultural chemistry, where it could be utilized in the development of new agrochemicals or as a component in existing formulations.
Used in Other Industrial Processes:
Due to its chemical properties, CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-, PHENYLMETHYL ESTER may also find use in other industrial processes, where its reactivity and functional groups can contribute to the synthesis of various products.
It is important to handle and use CARBAMIC ACID, N-(6-AMINO-2-PYRIDINYL)-, PHENYLMETHYL ESTER with caution and in accordance with proper safety protocols to ensure the safety of both individuals and the environment.

Upstream product

• 141-86-6 2.6-diaminopyridine 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 853058-08-9 6-(6-benzyloxycarbonylamino-pyridin-2-ylcarbamoyl)-4-decyloxy-pyridine-2-carboxylic acid methyl ester 
• 853058-10-3 6-(6-benzyloxycarbonylamino-pyridin-2-ylcarbamoyl)-4-decyloxy-pyridine-2-carboxylic acid 
• 853058-11-4 6-(6-{[6-(6-benzyloxycarbonylamino-pyridin-2-ylcarbamoyl)-4-decyloxy-pyridine-2-carbonyl]-amino}-pyridin-2-ylcarbamoyl)-4-decyloxy-pyridine-2-carboxylic acid methyl ester 
• 853058-13-6 6-(6-{[6-(6-benzyloxycarbonylamino-pyridin-2-ylcarbamoyl)-4-decyloxy-pyridine-2-carbonyl]-amino}-pyridin-2-ylcarbamoyl)-4-decyloxy-pyridine-2-carboxylic acid 

Relevant articles and documents

APOPTOSIS SIGNAL-REGULATING KINASE 1 INHIBITORS AND METHODS OF USE THEREOF

The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, ester, stereoisomer, tautomer, solvate, hydrate, or combination thereof: which inhibit the Apoptosis signal-regulating kinase 1 (ASK-1), which associated with autoimmune disorders, neurodegenerative disorders, inflammatory diseases, chronic kidney disease, cardiovascular disease. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from ASK-1 related disease. The invention also relates to methods of treating an ASK-1 related disease in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The present invention specifically relates to methods of treating ASK-1 associated with hepatic steatosis, including non-alcoholic fatty liver disease (NAFLD) and non-alcohol steatohepatitis disease (NASH).

Synthesis and properties of oligocarboxamide molecular strands containing 1,8-naphthyridine and pyridine groups

Oligocarboxamide molecular strands based on carboxamide between 1,8-naphthyridine and pyridine, pyridine and pyridine, 1,8-naphthyridine and benzene, and pyridine and benzene have been prepared. They have afforded various inclusion complexes with organic

Intramolecular versus intermolecular induction of helical handedness in pyridinedicarboxamide oligomers

A new convergent synthetic scheme has been developed to prepare oligoamides of 2,6-diaminopyridine and 4-decyloxy-2,6-pyridinedicarboxylic acid. These compounds adopt stable single helical conformations in solution. NMR and circular dichroism studies show