110429-24-8

Basic information

• Product Name: 2-Quinolinecarboxylic acid, 3-(phenylmethoxy)-
• CAS NO: 110429-24-8
• Molecular Formula: C17H13NO3
• Molecular Weight: 279.295
• Mol File: 110429-24-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Quinolinecarboxylic acid, 3-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Quinolinecarboxylic acid, 3-(phenylmethoxy)-(110429-24-8)
• EPA Substance Registry System: 2-Quinolinecarboxylic acid, 3-(phenylmethoxy)-(110429-24-8)

Safety Data

• Hazardous Substances Data: 110429-24-8(Hazardous Substances Data)

Upstream product

• 529-23-7 o-aminobenzaldehyde 
• 171917-54-7 Methyl 3-(benzyloxy)quinoline-2-carboxylate 
• 100-51-6 benzyl alcohol 

Downstream Products

• 171917-54-7 Methyl 3-(benzyloxy)quinoline-2-carboxylate 
• 15462-45-0 Methyl 3-hydroxyquinoline-2-carboxylate 
• 1515606-02-6 (N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)₂ 
• 174311-16-1 N¹-SES-N⁶-<<3-(benzyloxy)quinolyl>-2-carbonyl>-(D-Ser-Pip-Gly-Sar-NMe-Val)2(serine hydroxyl) dilactone 

Relevant articles and documents

Substituted quinoline-2-carboxamides, their preparation and their use as pharmaceuticals, and intermediates

The invention relates to substituted quinoline-2-carboxylic acid amides of the formula I STR1 their preparation and their use, and intermediates which are formed in the preparation of the compounds of the formula I. The compounds according to the inventio

Synthesis of key sandramycin analogs: Systematic examination of the intercalation chromophore

The preparation and examination of 2-22 constituting a systematic study of the chromophore of sandramycin (1) are detailed. Fluorescence quenching studies were used to establish binding constants for 1-24 within calf thymus DNA, within a single high affin

Modified Friedlander Condensation for the Synthesis of 3-Hydroxyquinoline-2-carboxylates

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