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Product Details
Chemical Properties |
white to beige or light tan adhering crystals or |
Uses |
Acetylating agent for capping unreacted amino groups in peptide synthesis. |
General Description |
Rate of solvolysis of 1-acetylimidazole in acid solutions was evaluated. Reaction of 1-acetylimidazole with orthophosphate and adenosine-5′-phosphate has been reported. |
Purification Methods |
It is recrystallised from isopropenyl acetate and dried in a vacuum over P2O5. [Riordan & Valee Methods Enzymol 25 500 1972, Beilstein 23/4 V 218.] |
InChI:InChI=1/C5H6N2O/c1-5(8)7-3-2-6-4-7/h2-4H,1H3
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1H-imidazole
4-nitrophenol acetate
N-Acetylimidazole
4-nitro-phenol
Conditions | Yield |
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With dm-3 borate buffer; at 25 ℃; Rate constant; pH 9.00; also in the presence of cyclodextrins at var conc.;
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With sodium dodecyl-sulfate; In water; acetonitrile; at 25 ℃; pH=8.92; Further Variations:; Reagents; Kinetics;
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In ethanol; water; Temperature; Activation energy; Kinetics; Mechanism;
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1H-imidazole
2,3-dichlorophenyl acetate
N-Acetylimidazole
2,3-dichlorophenol
Conditions | Yield |
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With sodium dodecyl-sulfate; In water; acetonitrile; at 25 ℃; pH=8.92; Kinetics;
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1H-imidazole
Isopropenyl acetate
acetyl chloride
1-Acetyl-4(1H)-pyridinon
1H-imidazole
acetic acid
N-((Z)-5-anilino-[1,2,4]dithiazol-3-ylidene)-acetamide
14-Fluor-vitamin-A-acetat
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