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7-Hydroxychlorpromazine, also known as 7-hydroxy-2-chloropromazine, is a significant metabolite of the atypical antipsychotic drug Chlorpromazine. It possesses various pharmacological properties, including antiadrenergic, antiserotonergic, anticholinergic, and antihistaminergic activities, which contribute to its therapeutic effects.

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  • 2095-62-7 Structure
  • Basic information

    1. Product Name: 7-hydroxychlorpromazine
    2. Synonyms: 7-hydroxychlorpromazine;7-Hydroxy-2-chloropromazine;NSC 131053
    3. CAS NO:2095-62-7
    4. Molecular Formula: C17H19ClN2OS
    5. Molecular Weight: 334.869
    6. EINECS: N/A
    7. Product Categories: Amines, Metabolites & Impurities, Neurochemicals, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
    8. Mol File: 2095-62-7.mol
  • Chemical Properties

    1. Melting Point: 178-179℃
    2. Boiling Point: 513.6°C at 760 mmHg
    3. Flash Point: 264.4°C
    4. Appearance: /
    5. Density: 1.281g/cm3
    6. Vapor Pressure: 3.59E-11mmHg at 25°C
    7. Refractive Index: 1.644
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 7-hydroxychlorpromazine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 7-hydroxychlorpromazine(2095-62-7)
    12. EPA Substance Registry System: 7-hydroxychlorpromazine(2095-62-7)
  • 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: 2095-62-7(Hazardous Substances Data)

2095-62-7 Usage

Uses

Used in Pharmaceutical Industry:
7-Hydroxychlorpromazine is used as an active metabolite for enhancing the therapeutic effects of Chlorpromazine in the treatment of schizophrenia. Its presence in the body helps to improve the overall efficacy of the antipsychotic medication by contributing to the modulation of various neurotransmitter systems involved in the disorder.
Used in Research and Development:
7-Hydroxychlorpromazine is utilized as a research compound for studying the pharmacological properties and mechanisms of action of Chlorpromazine. This helps in understanding the drug's effects on different neurotransmitter systems and its role in the treatment of schizophrenia and other related conditions.
Used in Drug Metabolism Studies:
7-Hydroxychlorpromazine serves as a key metabolite in the study of drug metabolism and pharmacokinetics of Chlorpromazine. Understanding its formation, distribution, and elimination in the body can provide valuable insights into the drug's safety, efficacy, and potential drug-drug interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 2095-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2095-62:
(6*2)+(5*0)+(4*9)+(3*5)+(2*6)+(1*2)=77
77 % 10 = 7
So 2095-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H19ClN2OS/c1-19(2)8-3-9-20-14-6-5-13(21)11-17(14)22-16-7-4-12(18)10-15(16)20/h4-7,10-11,21H,3,8-9H2,1-2H3

2095-62-7Relevant articles and documents

Bacterial Biosynthetic P450 Enzyme PikCD50N: A Potential Biocatalyst for the Preparation of Human Drug Metabolites

Cheng, Fangyuan,Du, Lei,Durairaj, Pradeepraj,Guo, Jiawei,Li, Fengwei,Li, Shengying,Liu, Xiaohui,Long, Xiangtian,Ma, Li,Tang, Dandan,Zhang, Gang,Zhang, Wei,Zhang, Xingwang

, p. 14563 - 14571 (2021/11/12)

Human drug metabolites (HDMs) are important chemicals widely used in drug-related studies. However, acquiring these enzyme-derived and regio-/stereo-selectively modified compounds through chemical approaches is complicated. PikC is a biosynthetic P450 enz

Synthesis of potential drug metabolites by a modified Udenfriend reaction

Slavik, Roger,Peters, Jens-Uwe,Giger, Rudolf,Bürkler, Markus,Bald, Eric

experimental part, p. 749 - 752 (2011/03/21)

The scope and the limitations of a modified Udenfriend reaction for the one-step synthesis of potential drug metabolites were explored. Several drugs (clozapine, chlorpromazine, imipramine, buspirone, diltiazem, and propranolol) were subjected to modified Udenfriend conditions (Fe2+/Mn 2+/EDTA/ascorbic acid/O2). From each reaction, one to four oxidation products were obtained in 1-8% overall yield. Many of these products (9 out of 14) have been reported to be metabolites of the parent drugs in vivo. The products resulted mainly from aromatic hydroxylation, and are not readily accessible by conventional synthesis. Thus, the described reaction may be useful in drug discovery whenever a facile synthetic access is more important than high yields (e.g., for a fast derivatisation of compounds or the preparation of metabolites). Poorly water-soluble compounds cannot be converted, which is an important limitation of this method. 2010 American Chemical Society.

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