23545-42-8 Usage
General Description
N-(2-Bromoethyl)-1,3-propanediamine dihydrobromide is a chemical compound known for its role as an intermediate in organic synthesis. It has the molecular formula C5H15Br3N2, indicating that it consists of five carbon atoms, 15 hydrogen atoms, three bromine atoms, and two nitrogen atoms. N-(2-Bromoethyl)-1,3-propanediamine dihydrobromide is characterized by its significant reactivity, a trait common to many bromine-containing compounds. Its properties also allow it to act as a precursor for the production of a wide variety of more complex molecules. Additionally, this compound is soluble in water, which can enhance the safety and convenience of handling and storage procedures. Its applications are found in diverse areas, including medicinal chemistry, materials science, and industrial manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 23545-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,4 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23545-42:
(7*2)+(6*3)+(5*5)+(4*4)+(3*5)+(2*4)+(1*2)=98
98 % 10 = 8
So 23545-42-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H13BrN2/c6-2-5-8-4-1-3-7/h8H,1-5,7H2
23545-42-8Relevant articles and documents
PROCESS FOR THE PREPARATION OF (ω -AMINOALKYLAMINO)ALKYL HALIDES AND CONVERSION TO AMIFOSTINE
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Page/Page column 10-11, (2008/06/13)
The present invention relates to processes for the preparation of (ω- aminoalkylainino)alkyl halides, their conversion to S-ω-(ω-aminoalkylamino)alkyl phosphothioates, and purification of the crystalline products of the reaction. The preparation process for the (ω-aminoalkylamino)alkyl halides comprises contacting an appropriate alcohol with a brominating agent in the presence of a sulfone solvent under temperature and pressure conditions suitable to effect salt formation without subsequent premature precipitation. The process is especially useful for converting (ω-aminoalkylamino)ethyl alcohol to amifostine.