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Structure

2-Methyl-1,8-naphthyridine-3-carboxylic acid monohydrate

CAS
387350-60-9
Catalog Number
ACM387350609
Category
Other Products
Molecular Weight
206.2
Molecular Formula
C10H10N2O3

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  • Product Description
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Specification

Synonyms
2-methyl-1,8-naphthyridine-3-carboxylic acid, 387350-60-9, AG-F-36580, Peakdale1_000001, PubChem14760, AC1MC6HT, AC1Q2PFI, SureCN125290, Ambpe3000001, CTK1C1419, HMS518A01, MolPort-000-159-652, ACT04389, SBB090759, AKOS006227664, 3-Carboxy-2-methyl-1,8-naphthyridine, FT-0687340, X3128, 1,8-Naphthyridine-3-carboxylicacid, 2-methyl-, 1,8-Diaza-2-methylnaphthalene-3-carboxylic acid
IUPAC Name
2-methyl-1,8-naphthyridine-3-carboxylic acid
Canonical SMILES
CC1=C(C=C2C=CC=NC2=N1)C(=O)O
InChI Key
STQOBEMCYUGNTL-UHFFFAOYSA-N
Boiling Point
356.3ºC at 760mmHg
Melting Point
191-195ºC
Flash Point
169.3ºC
Density
1.355g/cm³
Exact Mass
188.05900
Hazard Statements
Xi: Irritant;
H-Bond Acceptor
4
H-Bond Donor
1

Upstream Synthesis Route 1

  • 5174-88-9
  • 387350-60-9

Reference: [1]Ramesh; Sreenivasulu
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2004, vol. 43, # 4, p. 897 - 900]
[2]Location in patent: scheme or table
Ramesh; Thirumala Chary; Laxminarayana; Sreenivasulud
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2010, vol. 49, # 9, p. 1271 - 1273]

Downstream Synthesis Route 1

  • 387350-60-9
  • 258503-94-5

Reference: [1]Ramesh; Sreenivasulu
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2004, vol. 43, # 4, p. 897 - 900]
[2]Location in patent: scheme or table
Ramesh; Thirumala Chary; Laxminarayana; Sreenivasulud
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2010, vol. 49, # 9, p. 1271 - 1273]
[3]Current Patent Assignee: RESPIRATORIUS - US2016/101195, 2016, A1
Location in patent: Paragraph 0049-0050

Downstream Synthesis Route 2

  • 387350-60-9
  • 674333-39-2

Reference: [1]Ramesh; Sreenivasulu
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2004, vol. 43, # 4, p. 897 - 900]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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