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
• Article Data: 1

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

Chemical Properties

white crystalline powder

Uses

(R)-(+)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone is a chiral glycine derivative used for the synthesis of amino acids.

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

• 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 
• 137393-88-5 (5S,8R)-8-(t-butyl)-7-methyl-4,4-diphenyl-3-oxa-1,7-diazabicyclo<3.3.0>octan-2-one 

Relevant articles and documents

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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