1046832-15-8 Usage
Chemical Class
1-Methyl-[1,4]diazepane hydrochloride belongs to the class of diazepanes, which are heterocyclic compounds.
Appearance
It is typically found in the form of a white or off-white crystalline powder.
Solubility
It is soluble in water.
Use as a Precursor
It is commonly used as a precursor in the synthesis of pharmaceutical drugs.
Potential Applications
It has potential applications in the field of medicinal chemistry.
Pharmacological Effects
It has been studied for its potential pharmacological effects, including its ability to interact with certain neurotransmitter receptors in the brain.
Anticonvulsant Properties
It has been investigated for its potential anticonvulsant properties.
Sedative Properties
It has been investigated for its potential sedative properties.
Subject of Interest
It is a subject of interest for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1046832-15-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,8,3 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1046832-15:
(9*1)+(8*0)+(7*4)+(6*6)+(5*8)+(4*3)+(3*2)+(2*1)+(1*5)=138
138 % 10 = 8
So 1046832-15-8 is a valid CAS Registry Number.
1046832-15-8Relevant articles and documents
Process for preparing N-methyl homopiperazine from 2-haloethylamine compound
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Paragraph 0090-0093, (2017/12/27)
The invention discloses a process for preparing N-methyl homopiperazine from 2-haloethylamine compound, and the process comprises the following steps: Step 1, taking the 2-halogenated ethylamine compound as a raw materia to react with ethyl trifluoroacetate to obtain N-(2-Haloethyl) trifluoroacetamide; Step (2) taking the N-(2-Haloethyl) trifluoroacetamide as a raw material to react with methylamine or methylamine hydrochloride to obtain N-methyl-N'-trifluoroacetyl ethylenediamine; Step (3) taking the N-methyl-N'-trifluoroacetyl ethylenediamine as a raw material to react with 1,3-disubstituted propane compound to obtain N-methyl-N'-trifluoroacetyl homopiperazine; Step (4) taking the N-methyl-N'-trifluoroacetyl homopiperazine as a raw material to react with a hydrogen chloride ethanol solution to obtain N-methyl homopiperazine dihydrochloride; and Step (5) taking the N-methyl homopiperazine dihydrochloride as a raw material to prepare the N-methyl homopiperazine by alkalization. The process has the advantages of simple operation, low cost, high yield, low pollution and suitability for industrialized production.
