4-Chlorodehydromethyltestosterone

Base Information

• Chemical Name: 4-Chlorodehydromethyltestosterone
• CAS No.: 2446-23-3
• Deprecated CAS: 25466-33-5
• Molecular Formula: C₂₀H₂₇ClO₂
• Molecular Weight: 334.886
• UNII: ZPZ473F40K
• DSSTox Substance ID: DTXSID10179216
• Nikkaji Number: J507.800H
• Wikipedia: Chlorodehydromethyltestosterone
• Wikidata: Q909987
• Metabolomics Workbench ID: 38537
• Mol file: 2446-23-3.mol

Synonyms:4-chloro-methandienone;CDMT;D-4-chloro-17 beta-hydroxy-3-oxo-17 alpha-methylandrosta-1,4-diene;dehydrochlormethyltestosterone;Oral Turinabol;Turinabol-oral

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of 4-Chlorodehydromethyltestosterone

Chemical Property:

• Appearance/Colour: Off-white solid
• Vapor Pressure: 1.42E-10mmHg at 25°C
• Melting Point: 149-151 °C(Solv: acetone (67-64-1); hexane (110-54-3))
• Refractive Index: 1.579
• Boiling Point: 464.4 °C at 760mmHg
• PKA: 15.05±0.70(Predicted)
• Flash Point: 234.6 °C
• PSA: 0.00000
• Density: 1.2 g/cm³
• LogP: 9.32020
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 334.1699578
• Heavy Atom Count: 23
• Complexity: 636

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC12CCC3C(C1CCC2(C)O)CCC4=C(C(=O)C=CC34C)Cl
• Isomeric SMILES: C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(C)O)CCC4=C(C(=O)C=C[C@]34C)Cl
• Description: 4-Chlorodehydromethyltestosterone (CDMT; brand name Oral Turinabol), also known as Chlorodehydromethyltestosterone, is an anabolic–androgenic steroid (AAS). It is the 4-chloro-substituted derivative of metandienone (dehydromethyltestosterone). Turinabol is indicated for hormone replacement therapy in men suffering from androgen deficiency or in severe cases of catabolism.
• Uses: 4-Chlorodehydromethyltestosterone is a derivative of dehydrochloromethyltestosterone. Metabolite of anabolic steroids. it can produce quality gains in muscle mass as well as strength, even if these gains are not as dramatic or quick as you might get from an aromatizable, or more androgenic oral steroid.

Technology Process of 4-Chlorodehydromethyltestosterone

There total 2 articles about 4-Chlorodehydromethyltestosterone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 53.0%

4-chloro-17α-methylandrost-4-en-17β-ol-3-one (5785-58-0) → oral-turinabol (2446-23-3)

Guidance literature:

With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,4-dioxane; for 48h; Heating;

DOI:10.1016/0039-128X(95)00008-E

Reference yield:

→ 4-Chlor-1-dehydro-17α-methyl-testosteron (2446-23-3,87787-86-8)

Guidance literature:

/BRN= 296683/ u. Collidin;

upstream raw materials:

4-chloro-17α-methylandrost-4-en-17β-ol-3-one

Refernces

• 1、 SCHUBERT,STACHOWIAK,ONKEN,SPECHT,BARNIKOL-OETTLER,BODE,HELLER,POHNERT,SCHWARZ,ZEPTER. "ANABOLIC-ACTIVE STEROIDS.". . p. 323 - 331. Retrieved 2007/10/08.