3647-69-6 Usage
Description
4-(2-Chloroethyl)morpholine hydrochloride, also known as MOC, is a white to beige crystalline powder with chemical properties that make it a versatile intermediate in the synthesis of various compounds. It is primarily used in the pharmaceutical industry for the production of drugs with different therapeutic applications.
Uses
Used in Pharmaceutical Industry:
4-(2-Chloroethyl)morpholine hydrochloride is used as an intermediate for the synthesis of pharmaceuticals for various therapeutic applications. It plays a crucial role in the production of drugs such as floredil, morinamide, nimorazole, and pholcodine, which are used to treat a range of medical conditions.
Used in Anticancer Applications:
4-(2-Chloroethyl)morpholine is used in the preparation of potential DNA cross-linking antitumor agents. These agents have the ability to bind to DNA and disrupt its function, thereby inhibiting the growth and proliferation of cancer cells.
Used in Synthetic Opiate Analogues:
4-(2-Chloroethyl)morpholine is also used in the synthesis of synthetic opiate analogues, which are compounds that mimic the effects of natural opiates but can be designed to have specific therapeutic properties or reduced side effects.
Used in Sickle-Cell Anemia Treatment:
4-(2-Chloroethyl)morpholine may possess sickle-cell hemoglobin aggregation inhibiting activity, which could potentially be used in the development of treatments for sickle-cell anemia, a genetic disorder that affects red blood cells.
Used in Agrochemical Industry:
4-(2-Chloroethyl)morpholine hydrochloride (MOC) is used as an intermediate in the synthesis of agrochemicals, which are chemicals used in agriculture to enhance crop production and protect plants from pests and diseases.
Used in Dye Industry:
4-(2-Chloroethyl)morpholine hydrochloride (MOC) is also used as an intermediate for the synthesis of dyestuff intermediates, which are essential components in the production of various types of dyes used in different industries, such as textiles, plastics, and printing.
Safety Profile
Experimental
reproductive effects. Mutation data
reported. When heated to decomposition it
emits very toxic fumes of Cland NOx.
Check Digit Verification of cas no
The CAS Registry Mumber 3647-69-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3647-69:
(6*3)+(5*6)+(4*4)+(3*7)+(2*6)+(1*9)=106
106 % 10 = 6
So 3647-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H12ClNO/c7-1-2-8-3-5-9-6-4-8/h1-6H2/p+1
3647-69-6Relevant articles and documents
Coumadin female phenol split-ring analogue and its medical use
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Paragraph 0039-0041, (2017/10/06)
The invention relates to the field of pharmaceutical chemistry, in particular to a coumestrol open-ring analogue with structures as shown in general formulae I and II and a medical application thereof, especially an application to the preparation of drugs as angiogenesis inhibition and vascular disruption agents.
INDENOISOQUINOLINONE DERIVATIVES, MANUFACTURING METHOD AND MEDICAL USE THEREOF
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Paragraph 0074; 0075, (2013/04/13)
Indenoisoquinolinone derivatives (I), the manufacturing method and the medical use thereof, which belong to pharmaceutical chemistry and organic chemistry field, are disclosed. These compounds can be used for treating several medical symptoms related to postmenopausal syndrome, uterine fibers deterioration and aortic smooth muscle cells proliferation, especially ER-(+) depend breast cancer. Meanwhile, these compounds can also be used for treating glioma and lung cancer, and have inhibiting effect on tumor metastasis effect on tumor metastasis.
1,2,3,4,5,6-hexahydroazepino(4,5-B)indole derivatives, their preparation, intermediate compounds, and their application in therapeutics
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, (2008/06/13)
The invention is related to new 1,2,3,4,5,6-hexahydro-5-hydroyalkylazepino[4,5-b]-indole derivatives, of formula: STR1 in which R1 denotes a hydrogen atom, an alkyl radical, an alkenyl radical, a benzyl radical, an alkylamino radical of the type STR2 where the groups R' are either hydrogen atoms or alkyl radicals or form, together with the nitrogen atom to which they are attached, a heterocyclic nucleus of the morpholinyl, piperidinyl, pyrrolidinyl or piperazinyl type, and m is 2 or 3, R2 denotes a hydrogen atom or a benzoyl or acyl radical, R3 denotes a hydrogen atom or an alkyl or benzyl radical, R4 denotes a hydrogen or halogen atom, an alkyl radical an alkoxy radical or a trifluoromethyl radical, and n is 1 or 2, and the salts of addition to pharmaceutically acceptable acids, and to process for their preparation, to intermediates obtained and to their therapeutical use in treating mental disorders.