ChemicalBook--->CAS DataBase List--->13602-11-4

13602-11-4

13602-11-4 Structure

13602-11-4 Structure
IdentificationBack Directory
[Name]

methyl 6-methylpyridine-2-carboxylate
[CAS]

13602-11-4
[Synonyms]

NSC 109151
Methyl 6-methylpicolinate
6-Methylpicolinic Acid Methyl Ester
Methyl 6-methyl-2-pyridinecarboxylate
methyl 6-methylpyridine-2-carboxylate
METHYL-6-MENTHYPYRIDINE-2-CARBOXYLATE
Methyl6-Methylpyridine-2-carboxylate>
Methyl6-methylpyridine-2-carboxylate,96%
6-Methyl-2-pyridinecarboxylic acid methyl ester
Methyl 6-methylpyridine-2-carboxylate(13602-11-4)
2-Pyridinecarboxylic acid, 6-Methyl-, Methyl ester
2-Pyridinecarboxylicacid,6-methyl-,methylester(9CI)
methyl 6-methylpyridine-2-carboxylate ISO 9001:2015 REACH
[EINECS(EC#)]

237-085-0
[Molecular Formula]

C8H9NO2
[MDL Number]

MFCD06203670
[MOL File]

13602-11-4.mol
[Molecular Weight]

151.163
Chemical PropertiesBack Directory
[Melting point ]

18 °C
[Boiling point ]

242℃
[density ]

1.104
[refractive index ]

1.5160-1.5200
[Fp ]

100℃
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

powder to lump to clear liquid
[pka]

1.93±0.10(Predicted)
[color ]

White or Colorless to Light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

Methyl 6-Methylpyridine-2-carboxylate is a reagent used in the sunthesis of antitumor agents based upon the dihydropyrrolopyrazole compounds. Also used in the synthesis of quinazolinone TGF-β inhibitors.
[Synthesis]

Methanol

67-56-1

6-Methyl-2-pyridinecarboxylic acid

934-60-1

methyl 6-methylpyridine-2-carboxylate

13602-11-4

Step 2: 26.8 g (0.195 mol) of SOCl2 was slowly added dropwise to 100 mL of methanol at a low temperature of -10 °C while stirring was continued. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature and stirring was continued for 1 hour. Subsequently, 10 g of 6-methyl-2-pyridinecarboxylic acid (Compound 2) was added to the reaction system and the reaction was refluxed at 80 °C for 5 hours. Upon completion of the reaction, 10.2 g of methyl 6-methyl-2-pyridinecarboxylate (Compound 3) was obtained in 93% yield.

[References]

[1] Patent: CN105294552, 2016, A. Location in patent: Paragraph 0047; 0051
[2] Patent: WO2004/48383, 2004, A1. Location in patent: Page 40
[3] Patent: WO2004/48382, 2004, A1. Location in patent: Page 8
[4] Patent: WO2016/187308, 2016, A1. Location in patent: Paragraph 0349
[5] Patent: WO2012/80221, 2012, A1. Location in patent: Page/Page column 98
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 6-methylpyridine-2-carboxylate(13602-11-4)1HNMR
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