Welcome to LookChem.com Sign In|Join Free
  • or
1-Benzoyl-5-methyl-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-5-ol is a complex organic compound with a molecular formula of C18H17NO2. It is a derivative of benzo[cd]indol, a tricyclic aromatic compound with a benzene ring fused to an indole ring. The molecule features a benzoyl group (C6H5-CO-) attached to the 1-position, a methyl group (-CH3) at the 5-position, and a hydroxyl group (-OH) at the 5-position as well. 1-benzoyl-5-methyl-1,2,2a,3,4,5-hexahydro-benzo[cd]indol-5-ol is characterized by its hexahydro structure, indicating the presence of six hydrogen atoms in a cyclic arrangement. It is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of more complex molecules or as a compound with specific biological activities. Due to its structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest for further research and development in chemical and pharmaceutical applications.

2811-66-7

Post Buying Request

2811-66-7 Suppliers

Recommended suppliers

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

2811-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2811-66-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2811-66:
(6*2)+(5*8)+(4*1)+(3*1)+(2*6)+(1*6)=77
77 % 10 = 7
So 2811-66-7 is a valid CAS Registry Number.

2811-66-7Relevant academic research and scientific papers

Stereoselective Epoxidations and Electrophilic Additions to Partial Ergot Alkaloids and Conformationally-Fixed Styrenes. Experimental and Theoretical Modeling Evidence for the Importance of Torsional Steering as a Stereocontrol Element

Martinelli, Michael J.,Peterson, Barry C.,Khau, Vien V.,Hutchison, Darrell R.,Leanna, M. Robert,et al.

, p. 2204 - 2210 (1994)

Partial ergot alkaloid substrates and related conformationally-fixed styrenes undergo epoxidation, osmium tetraoxide dihydroxylation, and hydrobromination with a level of stereoselectivity which cannot be explained by steric control but is consistent with

Heteroannulation process

-

, (2008/06/13)

A heteroannulation process for preparing piperidones and tetrahydropyridones by reacting an appropriately substituted enamine with an acryloyl derivative wherein a leaving group occupies the carbonyl; a process for cleaving a 1-phenylethyl group from an a

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 2811-66-7