5967-73-7 Usage
Description
(R)-dimethyl(1-methyl-4-oxo-3,3-diphenylhexyl)ammonium chloride is a white solid compound with a complex chemical structure. It is characterized by its unique arrangement of atoms and functional groups, which contribute to its specific properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(R)-dimethyl(1-methyl-4-oxo-3,3-diphenylhexyl)ammonium chloride is used as an active pharmaceutical ingredient for the treatment of opioid dependence. Its chemical properties and interactions with biological systems make it a promising candidate for developing new therapies and medications to address this critical health issue.
As a component in the development of medications for opioid dependence, (R)-dimethyl(1-methyl-4-oxo-3,3-diphenylhexyl)ammonium chloride is utilized for its potential to modulate the effects of opioids in the body, helping to reduce cravings and withdrawal symptoms, and ultimately supporting the recovery process for individuals struggling with addiction.
Safety Profile
Poison by intravenous,
subcutaneous, and intraperitoneal routes.
Human systemic effects by ingestion:
hallucinations, distorted perceptions, and
analgesia. Caution: Abuse leads to
habituation or addiction. When heated to
decomposition it emits very toxic fumes of
Cland NOx. See also METHADONE
HYDROCHLORIDE.
Check Digit Verification of cas no
The CAS Registry Mumber 5967-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5967-73:
(6*5)+(5*9)+(4*6)+(3*7)+(2*7)+(1*3)=137
137 % 10 = 7
So 5967-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H27NO.ClH/c1-5-20(23)21(16-17(2)22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19;/h6-15,17H,5,16H2,1-4H3;1H/t17-;/m1./s1
5967-73-7Relevant articles and documents
SYNTHESIS OF LEVOMETHADONE HYDROCHLORIDE
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Paragraph 0109-0115, (2020/09/15)
A method for synthesizing levomethadone hydrochloride including producing (R)-2-(dimethylamino)propan-1-ol by reducing N,N-dimethyl-D-alanine using borax, forming (R)-1-chloro-N,N-dimethylpropane-2-amine hydrochloride by chlorinating the (R)-2-(dimethylamino)propan-1-ol, synthesizing levomethadone nitrile hydrochloride by mixing the (R)-1-chloro-N,N-dimethylpropane-2-amine and diphenylacetonitrile with potassium t-butoxide and producing levomethadone hydrochloride by exposing the levomethadone nitrile hydrochloride to a Grignard reagent.
"A NOVEL PROCESS FOR CHIRAL RESOLUTION OF HIGHLY PURE (6R)-6-(DIMETHYLAMINO)-4,4-DIPHENYL-3-HEPTANONE FROM RACEMIC METHADONE HYDROCHLORIDE"
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Page/Page column 12, (2016/07/27)
The present invention discloses an improved process for preparing pure (dimethylarnino)-4,4-diphenyl-3-heptanone and its hydrochloride salt.
Synthesis of optically active methadones, LAAM and bufuralol by lipase-catalysed acylations
Hull, Jonathan D.,Scheinmann, Feodor,Turner, Nicholas J.
, p. 567 - 576 (2007/10/03)
(R)- and (S)-Methadones and levo-α-acetylmethadol (LAAM) have been synthesised starting from lipase-catalysed acylation of dimethylaminopropan-2-ol. An approach to the synthesis of (R)-bufuralol is also presented.