119838-44-7

Basic information

• Product Name: (R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE
• Synonyms: (R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE;(R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE;(R)-(+)-1-(TERT-BUTOXYCARBONYL)-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINE;(R)-(+)-1-(TERT-BUTOXYCARBONYL)-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE;R-BOC-BMI;(R)-(+)-1-(TERT-BUTOXYCARBONYL)-2-T-BUT&;(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE 99%;(R)-(+)-1-(TERT-BUTOXYCARBONYL)-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE 99%
• CAS NO: 119838-44-7
• Molecular Formula: C₁₃H₂₄N₂O₃
• Molecular Weight: 256.34
• Mol File: 119838-44-7.mol

Chemical Properties

• Melting Point: 68-70 °C(lit.)
• Boiling Point: 399.58°C (rough estimate)
• Flash Point: 168.7°C
• Appearance: /
• Density: 1.0600 (rough estimate)
• Vapor Pressure: 3.15E-05mmHg at 25°C
• Refractive Index: 1.4365
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE(119838-44-7)
• EPA Substance Registry System: (R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE(119838-44-7)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 8-10
• Hazardous Substances Data: 119838-44-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE is used as a key intermediate for the synthesis of various amino acids, which are essential building blocks for the development of pharmaceutical compounds. Its chiral nature allows for the creation of enantiomerically pure drugs, which is crucial for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Chemical Synthesis:
In the field of chemical synthesis, (R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE serves as a versatile building block for the creation of complex organic molecules. Its unique structure and reactivity make it a valuable component in the synthesis of a wide range of compounds, including those with potential applications in various industries such as agriculture, materials science, and environmental science.
Used in Research and Development:
(R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE is also utilized in research and development settings, where it can be employed to study the properties and reactivity of chiral compounds. This knowledge can be applied to the design and synthesis of new molecules with specific biological activities or material properties, contributing to the advancement of various scientific fields.

InChI:InChI=1/C13H24N2O3/c1-12(2,3)10-14(7)9(16)8-15(10)11(17)18-13(4,5)6/h10H,8H2,1-7H3/t10-/m1/s1

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 101055-55-4 (+/-)-2-(tert-butyl)-3-methylimidazolidin-4-one 

Downstream Products

• 123052-86-8 C₂₀H₂₃⁽²⁾H₇N₂O₃ 
• 1357394-21-8 C₁₅H₂₀BrNO₅ 
• 1357394-23-0 C₁₇H₂₂BrNO₅ 
• 1357394-19-4 C₁₄H₁₈BrNO₅ 
• 1357394-18-3 C₂₀H₂₉BrN₂O₄ 
• 1357394-16-1 C₂₀H₂₉BrN₂O₄ 
• 1357394-15-0 C₂₀H₂₉BrN₂O₄ 
• 137393-97-6 1-t-butyl 5-methyl (2R,5R)-5-benzyl-2-(t-butyl)-3-methyl-1,5-imidazolidinedicarboxylate 
• 137394-16-2 t-butyl (2R,5S)-5-benzyl-2-(t-butyl)-3-methyl-1-imidazolidinecarboxylate 
• 137393-78-3 t-butyl (2R,5R)-5-benzyl-2-(t-butyl)-3-methyl-1-imidazolidinecarboxylate 
• 137393-99-8 1-t-butyl 5-methyl (2R,5R)-2-(t-butyl)-3-methyl-5-phenylseleno-1,5-imidazolidinedicarboxylate 
• 137393-98-7 1-t-butyl 5-methyl (2R,5R)-2-(t-butyl)-3-methyl-5-phenylthio-1,5-imidazolidinedicarboxylate 
• 137394-04-8 1-t-butyl (2R,4S,5R)-5-benzoyl-2-(t-butyl)-3-methyl-4-phenyl-1,5-imidazolidinedicarboxylate 
• 137394-06-0 t-butyl (2R,4S)-2-(t-butyl)-4-(1'-hydroxybenzyl)-3-methyl-5-oxo-1-imidazolidinecarboxylate 

Relevant articles and documents

Synthesis of functionalized benzoboroxoles for the construction of boronolectins

Adducts of peptides and arylboronic acids are attractive tools for the selective recognition of carbohydrates. These structures resemble at least some of the properties of natural carbohydrate binders and have therefore been termed lectin mimetics or boro