Welcome to LookChem.com Sign In|Join Free
  • or
5α-hydroxy-3β-p-toluenesulfonyloxycholestan-6-one is a complex organic compound with the molecular formula C28H42O4S. It is a steroidal ketone derivative, featuring a cholestane core structure with a hydroxyl group at the 5α position, a p-toluenesulfonyl group at the 3β position, and a ketone group at the 6 position. 5α-hydroxy-3β-p-toluenesulfonyloxycholestan-6-one is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique functional groups and structural features. The p-toluenesulfonyl group is a protecting group often used in organic synthesis to shield hydroxyl groups from unwanted reactions, while the ketone group can participate in various chemical transformations. The compound's specific properties and reactivity would depend on the context of its use and the reactions it undergoes.

2762-57-4

Post Buying Request

2762-57-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2762-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2762-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2762-57:
(6*2)+(5*7)+(4*6)+(3*2)+(2*5)+(1*7)=94
94 % 10 = 4
So 2762-57-4 is a valid CAS Registry Number.

2762-57-4Downstream Products

2762-57-4Relevant academic research and scientific papers

Synthesis and plant growth promoting activity of polyhydroxylated ketones bearing the 5α-hydroxy-6-oxo moiety and cholestane side chain

Rosado-Abón, Anielka,De Dios-Bravo, Guadalupe,Rodríguez-Sotres, Rogelio,Iglesias-Arteaga, Martín A.

, p. 461 - 466 (2012)

Three polyhydroxylated ketones bearing the 5α-hydroxy-6-oxo moiety were obtained from cholesterol. Two of them show plant growth promoting activity in the bean's second internode bioassay. The obtained results indicate that the presence of the 5α-hydroxy-

Synthesis of cytotoxic 6E-hydroximino-4-ene steroids: Structure/activity studies

Deive,Rodríguez,Jiménez

, p. 2612 - 2618 (2007/10/03)

In an effort to determine the pharmaceutical utility and the structural requirements for activity against various tumor cell lines, several 6E-hydroximino-4-ene steroids with different side chains and degrees of unsaturation on ring A were synthesized in our laboratory. Evaluation of the synthesized compounds for cytotoxicity against P-388, A-549, HT-29, and MEL-28 tumor cells revealed that some important structural features are required for activity. The presence of a cholesterol-type side chain, which appears to play a major role in determining the biological activity, the existence of a ketone functionality at C-3, and an elevated degree of oxidation on ring A all result in higher bioctivity than other structural motifs.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2762-57-4