Methyl 4-imidazolecarboxylate

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CAS:17325-26-7
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Methyl 4-imidazolecarboxylate manufacturers

Methyl 4-imidazolecarboxylate Basic information
Product Name:Methyl 4-imidazolecarboxylate
Synonyms:RARECHEM AL BF 0762;METHYL IMIDAZOLE-4-CARBOXYLATE;METHYL 4-IMIDAZOLECARBOXYLATE;Methyl 1H-imidazole-4-carboxylate;1H-Imidazole-4-carboxylic acid methyl ester;3H-Imidazole-4-carboxylic acid methyl ester;Methyl 4-imidazolecarboxylate,98%;Methyl 4-imidazolecarboxylate ,99%
CAS:17325-26-7
MF:C5H6N2O2
MW:126.11
EINECS:626-673-6
Product Categories:Chemical Synthesis;Heterocyclic Building Blocks;Building Blocks;Building Blocks;Heterocyclic Building Blocks;Imidazoles;pharmacetical;Heterocyclic Compounds;Heterocycle
Mol File:17325-26-7.mol
Methyl 4-imidazolecarboxylate Structure
Methyl 4-imidazolecarboxylate Chemical Properties
Melting point 154-156 °C (lit.)
Boiling point 318.2±15.0 °C(Predicted)
density 1.46 g/cm3
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form Crystalline Powder
pka10.89±0.10(Predicted)
color White
InChIInChI=1S/C5H6N2O2/c1-9-5(8)4-2-6-3-7-4/h2-3H,1H3,(H,6,7)
InChIKeyDVLGIQNHKLWSRU-UHFFFAOYSA-N
SMILESC1NC(C(OC)=O)=CN=1
CAS DataBase Reference17325-26-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29332900
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
Methyl 4-imidazolecarboxylate Usage And Synthesis
Chemical PropertiesWhite crystalline powder
UsesMethyl 4-imidazolecarboxylate was used as a starting material in the synthesis of 1-(3-prop-1-enyl)-imidazole-4-carboxyaldehyde and osmium(2,2′-bipyridyl)2(methyl 4-imidazolcarboxylate)dichloride.
General DescriptionMethyl 4-imidazolecarboxylate is an alkyl ester of imidazole carboxylic acid.
Synthesis
Methanol

67-56-1

1H-Imidazole-4-carboxylic acid

1072-84-0

Methyl 4-imidazolecarboxylate

17325-26-7

Step 1 Synthesis of methyl 1H-imidazole-4-carboxylate: 1H-imidazole-4-carboxylic acid (1.0 g, 8.9 mmol) was mixed with concentrated sulfuric acid (1 mL) in methanol (30 mL), stirred and heated to 0 °C. The reaction mixture was reacted under reflux conditions overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and subsequently partitioned between cold water and ethyl acetate. The organic layer was separated and concentrated under reduced pressure to afford methyl 1H-imidazole-4-carboxylate (1 g, 89% yield).

References[1] Patent: US2010/160323, 2010, A1. Location in patent: Page/Page column 23-24
[2] Patent: CN108314654, 2018, A. Location in patent: Paragraph 0086-0088
[3] Inorganic Chemistry Communications, 2017, vol. 78, p. 32 - 36
[4] Patent: WO2012/143599, 2012, A1. Location in patent: Page/Page column 79
Methyl 4-imidazolecarboxylate Preparation Products And Raw materials
Raw materials1H-Imidazole-4-carboxylic acid-->1H-Imidazole-4-carbaldehyde-->Methyl, azo--->Methanol
Preparation ProductsImidazole-4-methanol
Tag:Methyl 4-imidazolecarboxylate(17325-26-7) Related Product Information
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