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(R)-Lormetazepam, a benzodiazepine-class medication, is utilized for treating anxiety and insomnia. It operates by augmenting the effects of the neurotransmitter GABA in the brain, leading to a calming and sedative impact. Due to the potential for tolerance, dependence, and withdrawal symptoms, it is generally prescribed for short-term use. Possible side effects include drowsiness, dizziness, and impaired coordination. It is crucial to adhere to the guidance of a healthcare professional when using this medication to minimize risks.

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  • 113679-56-4 Structure
  • Basic information

    1. Product Name: (R)-Lormetazepam
    2. Synonyms: (R)-Lormetazepam;2H-1,4-Benzodiazepin-2-one, 7-chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy-1-methyl-, (3R)- (9CI);2H-1,4-Benzodiazepin-2-one, 7-chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy-1-methyl-, (R)-
    3. CAS NO:113679-56-4
    4. Molecular Formula: C16H12 Cl2 N2 O2
    5. Molecular Weight: 335.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113679-56-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-Lormetazepam(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-Lormetazepam(113679-56-4)
    11. EPA Substance Registry System: (R)-Lormetazepam(113679-56-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 113679-56-4(Hazardous Substances Data)

113679-56-4 Usage

Uses

Used in Pharmaceutical Industry:
(R)-Lormetazepam is used as a therapeutic agent for treating anxiety and insomnia. It enhances the calming and sedative effects of GABA in the brain, providing relief from these conditions. However, its use is typically limited to short-term due to the risk of tolerance, dependence, and withdrawal symptoms associated with prolonged use.

Check Digit Verification of cas no

The CAS Registry Mumber 113679-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,7 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113679-56:
(8*1)+(7*1)+(6*3)+(5*6)+(4*7)+(3*9)+(2*5)+(1*6)=134
134 % 10 = 4
So 113679-56-4 is a valid CAS Registry Number.

113679-56-4Upstream product

113679-56-4Downstream Products

113679-56-4Relevant articles and documents

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

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Page/Page column 45-49; 56, (2010/12/31)

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.

THERMALLY IMMOBILIZED POLYSACCHARIDE DERIVATIVES

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Page 11, (2008/06/13)

The invention essentially relates to thermally crosslinked polysaccharide derivatives which contained no polymerizable functional groups prior to crosslinking and which are used in particular as support materials for the chromatographic separation of enantiomers. The present invention relates to thermally crosslinked polysaccharide derivatives in which the OH groups, as OR groups, have been esterified or converted into a carbamate (urethane), or mixtures of these, with the proviso that the OR groups contained no polymerizable double bonds prior to crosslinking. The thermally crosslinked polysaccharides according to the invention in conditioned form can also be used as pure polymers for the chromatographic separation of enantiomers.

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