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1,1-Diethoxy-2-isocyanoethane, with the molecular formula C7H13NO2 and a molecular weight of 143.18 g/mol, is a colorless liquid characterized by a pungent odor. It is a versatile reagent in organic synthesis, known for its reactivity in various chemical reactions such as nucleophilic addition, substitution, and rearrangement. 1,1-DIETHOXY-2-ISOCYANOETHANE is a valuable building block in the synthesis of complex organic molecules, heterocyclic compounds, and organic materials, contributing to the production of pharmaceuticals, agrochemicals, and other fine chemicals.

15586-32-0

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15586-32-0 Usage

Uses

Used in Pharmaceutical Industry:
1,1-Diethoxy-2-isocyanoethane is used as a reagent and building block for the synthesis of pharmaceuticals, due to its ability to participate in a range of chemical reactions that facilitate the creation of complex organic molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 1,1-Diethoxy-2-isocyanoethane serves as a key intermediate in the production of various agrochemicals, leveraging its versatile reactivity to form essential components of pesticides and other agricultural chemicals.
Used in Organic Synthesis:
1,1-Diethoxy-2-isocyanoethane is utilized as a reagent in organic synthesis for the preparation of heterocyclic compounds and organic materials, taking advantage of its capacity to undergo multiple types of chemical reactions, which is crucial for the development of new chemical entities.
Used in Research:
1,1-DIETHOXY-2-ISOCYANOETHANE is also used in research settings to explore novel chemical reactions and mechanisms, contributing to the advancement of organic chemistry and the discovery of new synthetic pathways.

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

15586-32-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-Diethoxy-2-isocyanoethane

1.2 Other means of identification

Product number -
Other names Isocynacetaldehyd-diethylacetal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15586-32-0 SDS

15586-32-0Relevant academic research and scientific papers

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.

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