141345-35-9

Basic information

• Product Name: 1H-Imidazole-1-carboxylic acid, 4,5-dihydro-4,4-dimethyl-, phenylmethyl ester
• CAS NO: 141345-35-9
• Molecular Formula: C13H16N2O2
• Molecular Weight: 232.282
• Mol File: 141345-35-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole-1-carboxylic acid, 4,5-dihydro-4,4-dimethyl-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-1-carboxylic acid, 4,5-dihydro-4,4-dimethyl-, phenylmethyl ester(141345-35-9)
• EPA Substance Registry System: 1H-Imidazole-1-carboxylic acid, 4,5-dihydro-4,4-dimethyl-, phenylmethyl ester(141345-35-9)

Safety Data

• Hazardous Substances Data: 141345-35-9(Hazardous Substances Data)

Usage

Molecular weight

241.29 g/mol

Structure

The compound has a five-membered imidazole ring with a carboxylic acid group at the 1-position, a phenylmethyl ester group at the 4-position, and two methyl groups at the 4,5-dihydro positions.

Functional groups

Imidazole ring, carboxylic acid, ester, phenyl, and methyl groups.

Appearance

The compound is likely to be a solid or a viscous liquid.

Solubility

It is expected to be soluble in organic solvents such as ethanol, methanol, and acetone, but insoluble in water.

Reactivity

The compound may react with strong acids, strong bases, and nucleophiles due to the presence of the ester and imidazole groups.

Stability

It is likely to be stable under normal conditions, but sensitive to heat, light, and moisture.

Applications

The compound may be used in the field of organic chemistry, pharmaceuticals, or material science, but further research is needed to determine its specific applications.

Safety

It is important to handle and use this compound with caution, following proper safety protocols and regulations, as it may have potential hazards such as irritancy, toxicity, or flammability.
Please note that this information is based on the provided material and general knowledge of chemical properties. Further experimental data and analysis may be required to confirm these properties and determine the specific applications of the compound.

Upstream product

• 119072-55-8 tert-butylisonitrile 
• 501-53-1 benzyl chloroformate 
• 2305-59-1 4,4-dimethyl-2-imidazoline 

Downstream Products

• 141345-39-3 (5R^*,6R^*)-4-(benzyloxycarbonyl)-6-(benzyloxy)-2,2,6-trimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one 
• 141345-41-7 (5R^*,6R^*)-4-(benzyloxycarbonyl)-2,2-dimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one-6-spiro-2'-tetrahydrofuran 
• 141345-37-1 (5R^*,6R^*)-4-(benzyloxycarbonyl)-6-methoxy-2,2,6-trimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one 
• 141345-45-1 (5S^*,6R^*)-6-(benzyloxy)-2,2,6-trimethyl-1,4-diazabicyclo<3.2.0>heptan-7-one 
• 141345-51-9 hexahydro-3,3,6-trimethyl-6-(phenylmethoxy)-5H-1,4-diazepin-5-one 
• 544481-02-9 quinoxaline-2-carboxylic acid 4-benzyloxycarbonyl-2,2,6-trimethyl-7-oxo-1,4-diaza-bicyclo[3.2.0]hept-6-yl ester 
• 544481-05-2 2,2,6-trimethyl-7-oxo-6-(quinoxalin-2-ylmethoxy)-1,4-diaza-bicyclo[3.2.0]heptane-4-carboxylic acid benzyl ester 
• 544481-01-8 6-hydroxy-2,2,6-trimethyl-7-oxo-1,4-diaza-bicyclo[3.2.0]heptane-4-carboxylic acid benzyl ester 
• 544481-00-7 6-(4-methoxy-benzyloxy)-2,2,6-trimethyl-7-oxo-1,4-diaza-bicyclo[3.2.0]heptane-4-carboxylic acid benzyl ester 

Relevant articles and documents

Synthesis and complexation properties of poly(ethylene glycol)-linked mono- and bis-dioxocyclams

Both tri- and tetra(ethylene glycol) linked bis-chromium carbene complexes have been synthesized. These carbene complexes were photolyzed with N-protected imidazolines to give protected azapenams. These were transformed into polyether-linked basket dioxocyclams 4a,b and bis-dioxocyclams 5a,b. These compounds have cavities for the complexation of both 'hard' and 'soft' metal ions. The complexes of Ni, Ba, and Gd were synthesized.