Cas no 41714-53-8 ((5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan)

(5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan structure
41714-53-8 structure
Product Name:(5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan
CAS No:41714-53-8
MF:C19H25NO3
MW:315.406705617905
CID:927301
PubChem ID:20833250
Update Time:2025-10-21

(5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan Chemical and Physical Properties

Names and Identifiers

    • Tetrahydrothebaine
    • 4,5alpha-Epoxy-3,6-dimethoxy-17-methylmorphinan
    • (5R,6S,9R,13S,14R)-4,5-Epoxy-3,6-dimethoxy-9alpha-methylmorphinan
    • Morphinan, 4,5-alpha-epoxy-3,6-dimethoxy-17-methyl-
    • (5alpha)-3,6-dimethoxy-17-methyl-4,5-epoxymorphinan
    • (4R,4aR,7aR,12bS)-7,9-dimethoxy-3-methyl-2,4,4a,5,6,7,7a,13-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline
    • (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan
    • NS00057882
    • 6-epi-Tetrahydrothebaine
    • SCHEMBL12744925
    • DTXSID90961919
    • EINECS 255-511-3
    • SCHEMBL16279825
    • 41714-53-8
    • 3,6-Dimethoxy-17-methyl-4,5-epoxymorphinan
    • Inchi: 1S/C19H25NO3/c1-20-9-8-19-12-5-7-15(22-3)18(19)23-17-14(21-2)6-4-11(16(17)19)10-13(12)20/h4,6,12-13,15,18H,5,7-10H2,1-3H3/t12-,13+,15?,18-,19-/m0/s1
    • InChI Key: RVJQWONQPCTLDL-SEYRRXLCSA-N
    • SMILES: O1C2=C(C=CC3C[C@@H]4[C@@H]5CCC([C@H]1[C@@]5(C=32)CCN4C)OC)OC

Computed Properties

  • Exact Mass: 315.183444
  • Monoisotopic Mass: 315.183444
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 2
  • Complexity: 485
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 4
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 30.9
  • XLogP3: 2.7

Experimental Properties

  • Density: 1.24
  • Boiling Point: 438.2°C at 760 mmHg
  • Flash Point: 128.6°C
  • Refractive Index: 1.606

(5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHENG KE LU SI SHENG WU JI SHU
sc-473665-2.5 mg
Tetrahydrothebaine,
41714-53-8
2.5 mg
¥3,234.00 2023-07-10
SHENG KE LU SI SHENG WU JI SHU
sc-473665-2.5mg
Tetrahydrothebaine,
41714-53-8
2.5mg
¥3234.00 2023-09-05

Additional information on (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan

Comprehensive Overview of (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan (CAS No. 41714-53-8)

(5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan, also known by its CAS number 41714-53-8, is a synthetic compound that belongs to the class of morphinans. This compound is of significant interest in the fields of medicinal chemistry and pharmacology due to its unique structural features and potential therapeutic applications. In this comprehensive overview, we will delve into the chemical properties, biological activities, and recent research advancements related to this compound.

The chemical structure of (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan is characterized by a morphinan skeleton with specific functional groups. The presence of an epoxy group at positions 4 and 5, along with methoxy groups at positions 3 and 6, and a methyl group at position 17, contributes to its distinct chemical properties. These structural features play a crucial role in determining the compound's biological activity and potential therapeutic applications.

Recent studies have focused on the pharmacological properties of (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan. One notable area of research is its interaction with opioid receptors. Opioid receptors are a family of G protein-coupled receptors that are involved in pain modulation and other physiological processes. Studies have shown that (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan exhibits selective binding to specific opioid receptor subtypes, which may have implications for the development of novel analgesic agents.

In addition to its potential as an analgesic, (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan has been investigated for its anti-inflammatory properties. Inflammation is a complex biological response to harmful stimuli and is associated with various diseases. Research has demonstrated that this compound can modulate inflammatory pathways by inhibiting the production of pro-inflammatory cytokines and reducing oxidative stress. These findings suggest that (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan may have therapeutic potential in treating inflammatory conditions.

The safety profile of (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan is another important aspect of its evaluation. Preclinical studies have assessed its toxicity and side effects in various animal models. Results indicate that this compound exhibits a favorable safety profile at therapeutic doses. However, further research is needed to fully understand its long-term effects and potential interactions with other drugs.

Clinical trials are essential for translating preclinical findings into practical applications. While there are currently no large-scale clinical trials specifically focused on (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan, several smaller studies have provided valuable insights into its efficacy and safety in human subjects. These trials have shown promising results in terms of pain relief and anti-inflammatory effects, paving the way for more extensive clinical investigations.

The synthesis of (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan is a complex process that requires precise control over reaction conditions. Various synthetic routes have been developed to produce this compound efficiently. One common approach involves the use of chiral catalysts to ensure the correct stereochemistry at key positions. Advances in synthetic chemistry have led to improved yields and purity levels, making it more feasible to produce this compound on a larger scale for research and potential commercial applications.

In conclusion, (5alpha,6beta)-4,5-epoxy-3,6-dimethoxy-17-methylmorphinan (CAS No. 41714-53-8) is a promising compound with potential therapeutic applications in pain management and inflammation treatment. Its unique chemical structure and pharmacological properties make it an attractive target for further research and development. As ongoing studies continue to uncover new insights into its mechanisms of action and safety profile, it holds significant promise for improving patient outcomes in various medical conditions.

Recommended suppliers
上海帛亦醫(yī)藥科技有限公司
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
SunaTech Inc.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
SunaTech Inc.
Hangzhou Cedareal Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Hangzhou Cedareal Technology Co., Ltd.
Hubei Cuiyuan Biotechnology Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hubei Cuiyuan Biotechnology Co.,Ltd
Shaanxi pure crystal photoelectric technology co. LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shaanxi pure crystal photoelectric technology co. LTD