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1-Propyl-1-(2-hydroxyethyl)aziridinium chloride is a complex organic compound with the chemical formula C6H14ClNO. It is a derivative of aziridinium, a heterocyclic compound containing a nitrogen atom in a three-membered ring. This specific compound features a propyl group (three-carbon alkyl chain) and a hydroxyethyl group (two-carbon chain with a hydroxyl group) attached to the nitrogen atom. The chloride ion (Cl-) is present as a counterion, making the compound a salt. It is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its potential reactivity and toxicity, it is essential to handle 1-propyl-1-(2-hydroxyethyl)aziridinium chloride with caution and in accordance with proper safety protocols.

99748-87-5

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99748-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99748-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,4 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99748-87:
(7*9)+(6*9)+(5*7)+(4*4)+(3*8)+(2*8)+(1*7)=215
215 % 10 = 5
So 99748-87-5 is a valid CAS Registry Number.

99748-87-5Downstream Products

99748-87-5Relevant academic research and scientific papers

Neurochemistry of aging. 1. Toxins for an animal model of Alzheimer's disease

Mistry,Abraham,Hanin

, p. 376 - 380 (1986)

A chronic deficiency in central cholinergic function has been implicated in a number of neuropsychiatric diseases including Alzheimer's disease. Until recently, animal models that simulate the neurochemical conditions that appear to cause these diseases in humans, as a result of a direct manipulation of the central cholinergic system, were not available. Over the past few years, however, we have been successful in developing a cholinotoxin, 1-ethyl-1-(2-hydroxyethyl)aziridinium chloride (AF64A), which has the potential to serve as a novel compound in developing animal models of human brain disorders in which a cholinergic hypofunction has been implicated. In this paper are described the design, synthesis, and testing of several structural analogues of AF64A as potential cholinotoxins, by evaluating them for their ability to inhibit high-affinity choline transport and their affinity toward brain muscarinic receptors. One of the compounds, 1-cyclopropyl-1-(2-hydroxyethyl)aziridinium chloride was found to have a remarkably high affinity (about 40 times higher than AF64A) toward brain muscarinic receptors.

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