15586-32-0 Usage
General Description
1,1-Diethoxy-2-isocyanoethane is a chemical compound with the molecular formula C7H13NO2 and a molecular weight of 143.18 g/mol. It is a colorless liquid with a pungent odor, and is commonly used as a reagent in organic synthesis. 1,1-Diethoxy-2-isocyanoethane is known for its versatile reactivity, and is used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a building block in the synthesis of complex organic molecules, and has found applications in the preparation of various heterocyclic compounds and organic materials. Additionally, it is known to undergo several types of chemical reactions, including nucleophilic addition, substitution, and rearrangement reactions. Overall, 1,1-Diethoxy-2-isocyanoethane is a valuable and widely used chemical in organic synthesis and research.
Check Digit Verification of cas no
The CAS Registry Mumber 15586-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15586-32:
(7*1)+(6*5)+(5*5)+(4*8)+(3*6)+(2*3)+(1*2)=120
120 % 10 = 0
So 15586-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2/c1-4-9-7(6-8-3)10-5-2/h7H,4-6H2,1-2H3
15586-32-0Relevant articles and documents
A new and general method for the synthesis of tripeptide aldehydes based on the multi-component Ugi reaction
Mroczkiewicz, Micha?,Ostaszewski, Ryszard
experimental part, p. 4025 - 4034 (2009/09/30)
Tripeptide aldehydes, such as Z-Leu-Leu-Leu-H (MG-132), are an important class of compounds due to their biological activity. A new, general method for the synthesis of tripeptide aldehydes based on the multi-component Ugi reaction was developed. A careful choice of isocyanides makes it possible to obtain tripeptide precursors whose functionalization led to target structures. This method can be used for the preparation of tripeptide aldehydes with non-natural amino acid side chains.
A FACILE SYNTHESIS OF 1-ARYL-2-ARYLTHIO-1H-IMIDAZOLES
Bossio, Ricardo,Marcaccini, Stefano,Pepino, Roberto,Polo, Cecilia,Torroba, Tomas
, p. 1287 - 1290 (2007/10/02)
The reaction between the hitherto unknown 2,2-diethoxy-1-isocyanoethane (1) with sulfenyl chlorides (2) and arylamines afforded isothioureas (4) which were cyclized to give the title compounds.
