1-Acetylimidazole

1-Acetylimidazole Basic information
Product Name:1-Acetylimidazole
Synonyms:1-Acetylimidazole98%;N-Acetylimidazole,98%;N-ACETYLIMIDAZOL;N-ACETYLIMIDAZOLE extrapure AR;1-Imidazolylmethyl ketone;1-(1H-Imidazole-1-yl)ethanone;1-Acetylimidazole ,99%;1-AcetliMidazole
CAS:2466-76-4
MF:C5H6N2O
MW:110.11
EINECS:219-577-7
Product Categories:amino;ImidazolesProtein Modification;Reagents for tyrosine modification;Building Blocks;Heterocyclic Building Blocks;Specific Amino Acid Modification;Acylation (GC Derivatizing Reagents);GC Derivatizing Reagents;Analytical Chemistry;Imidazoles
Mol File:2466-76-4.mol
1-Acetylimidazole Structure
1-Acetylimidazole Chemical Properties
Melting point 99-105 °C (lit.)
Boiling point 206.4°C (rough estimate)
density 1.2111 (rough estimate)
refractive index 1.4800 (estimate)
storage temp. 2-8°C
solubility water: soluble50mg/mL, clear, colorless
form Adhering Crystals or Crystalline Powder
pkapKa 3.6(H2O,t = 25,I=0.2) (Uncertain)
color White to beige or light tan
Water Solubility Hydrolyzes in water. Solubility in methanol (almost transparency).
Sensitive Moisture Sensitive
BRN 108425
Stability:Moisture Sensitive
CAS DataBase Reference2466-76-4(CAS DataBase Reference)
NIST Chemistry Reference1H-Imidazole, 1-acetyl-(2466-76-4)
EPA Substance Registry System1H-Imidazole, 1-acetyl- (2466-76-4)
Safety Information
Risk Statements 36/37/38
Safety Statements 24/25
WGK Germany 3
RTECS NI3400000
10-21
TSCA Yes
HS Code 29332900
MSDS Information
ProviderLanguage
NAI English
SigmaAldrich English
ACROS English
ALFA English
1-Acetylimidazole Usage And Synthesis
Chemical Propertieswhite to beige or light tan adhering crystals or
UsesRelatively specific reagent for tyrosyl residue acetylation. Reagent used in the synthesis of annulated imidazole derivatives.
UsesAcetylating agent for capping unreacted amino groups in peptide synthesis.
UsesIt is a mild acylating agent and its reactivity can be enhanced by quaternization with, e.g. benzyl bromide. 1-Acetylimidazole was used as acetylation reagent for amino groups. It was also employed for acetylation of histones. It is relatively specific reagent for tyrosyl residue acetylatioa dn a reagent used in the synthesis of annulated imidazole derivatives.
DefinitionChEBI: N-acetylimidazole is a N-acylimidazole.
General DescriptionRate of solvolysis of 1-acetylimidazole in acid solutions was evaluated. Reaction of 1-acetylimidazole with orthophosphate and adenosine-5′-phosphate has been reported.
Purification MethodsIt is recrystallised from isopropenyl acetate and dried in a vacuum over P2O5. [Riordan & Valee Methods Enzymol 25 500 1972, Beilstein 23/4 V 218.]
IMIDAZO[1,2-B]ISOQUINOLINE-5,10-DIONE Imidazol-1-yl-acetic acid 2-Methyl-5-Acetylimidazole N-ACETYL-L-TYROSINE ETHYL ESTER 4-ACETYLIMIDAZOLE-2-CARBOXYLIC ACID METHYL ESTER Vat Orange 7 tributyl acetocitrate THIAZOLO(2 3-B)BENZIMIDAZOLE-3(2H)-ONE N-PENTAFLUOROBENZOYLIMIDAZOLE 1-PROPIONYLIMIDAZOLE (2-CHLOROPHENYL)(4,5-DICHLORO-1H-IMIDAZOL-1-YL)METHANONE Vat Red 15 fluorescein n-acetylimidazole (4,5-DICHLORO-1H-IMIDAZOL-1-YL)(2-THIENYL)METHANONE THEOPHYLLINE-8-BUTYRIC ACID LACTAM 1-(PENTAFLUOROPROPIONYL)IMIDAZOLE BENZIMIDAZO[2,1-A]BENZ[D,E]ISOQUINOLION-7-ONE Acetylimidazole diethyl acetal

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