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Ethane-1,2-diyl diaziridine-1-carboxylate is a chemical compound that is a diaziridine derivative, containing a diaziridine ring and a carboxylate functional group. It is known for its reactivity, particularly under ultraviolet light, and is utilized in various scientific applications.
Used in Photoaffinity Labeling Studies:
Ethane-1,2-diyl diaziridine-1-carboxylate is used as a photoaffinity probe for investigating protein-protein interactions and protein-ligand interactions. The reason for its use is that upon exposure to ultraviolet light, it undergoes a photochemical reaction, leading to the formation of a highly reactive carbene species. This reactive species can covalently attach to nearby biomolecules, allowing researchers to selectively label and identify binding partners of the target protein.
Used in Biological Pathway Research:
Ethane-1,2-diyl diaziridine-1-carboxylate is used as a research tool for studying biological pathways. The application reason is that the selective labeling of target proteins and their binding partners provides valuable information that can help elucidate the mechanisms of action and interactions within complex biological systems.
Used in Drug Development:
Ethane-1,2-diaziridine-1-carboxylate is used as a compound in the development of new drugs. The application reason is that its ability to form covalent bonds with biomolecules can be harnessed to identify potential drug targets and to understand the interactions between drugs and their targets, which is crucial for the design of effective therapeutic agents.
Used in Photochemical Reactions:
Ethane-1,2-diaziridine-1-carboxylate is used as a reactant in photochemical reactions. The application reason is its propensity to form reactive carbene species upon exposure to ultraviolet light, which can be used to study the reactivity of such species and their potential applications in synthetic chemistry and materials science.
Safety Note:
When handling ethane-1,2-diyl diaziridine-1-carboxylate, caution should be taken due to its potential reactivity and toxicity. Proper safety measures and protocols should be followed to minimize risks associated with its use.

881-92-5

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881-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881-92-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 881-92:
(5*8)+(4*8)+(3*1)+(2*9)+(1*2)=95
95 % 10 = 5
So 881-92-5 is a valid CAS Registry Number.

881-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(aziridine-1-carbonyloxy)ethyl aziridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names aziridine-1-carboxylic acid ethane-1,2-diyl ester

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:881-92-5 SDS

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