Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6722-06-1

6,11-Dihydro[1]benzopyrano[4,3-b]indole is a complex organic chemical compound with the molecular formula C16H13NO. It is a derivative of the indole alkaloid class, characterized by the fusion of a benzopyran ring to the indole structure. 6,11-Dihydro[1]benzopyrano[4,3-b]indole is known for its potential biological activities and is often found in the context of natural products chemistry, particularly in the study of plant alkaloids. It may also be of interest in the field of medicinal chemistry due to its structural features that could interact with biological targets. The compound's specific applications and properties are subject to ongoing research, and its synthesis and analysis are typically carried out by chemists using advanced techniques in organic synthesis and spectroscopy.

6722-06-1

Post Buying Request

6722-06-1 Suppliers

Recommended suppliersmore

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

6722-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6722-06-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6722-06:
(6*6)+(5*7)+(4*2)+(3*2)+(2*0)+(1*6)=91
91 % 10 = 1
So 6722-06-1 is a valid CAS Registry Number.

6722-06-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,11-dihydrochromeno[4,3'-b]indole

1.2 Other means of identification

Product number -
Other names 6,11-dihydrochromeno[4,3-b]indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6722-06-1 SDS

6722-06-1Downstream Products

6722-06-1Relevant articles and documents

Thiourea-catalyzed enantioselective addition of indoles to pyrones: Alkaloid cores with quaternary carbons

Yeung, Charles S.,Ziegler, Robert E.,Porco, John A.,Jacobsen, Eric N.

supporting information, p. 13614 - 13617 (2015/02/05)

We report the development of a catalytic method for the enantioselective addition of indoles to pyrone-derived electrophiles. Arylpyrrolidino-derived thioureas catalyze the addition with high stereoselectivity in the presence of catalytic quantities of an achiral Bronsted acid. The indole-pyrone adducts feature a quaternary stereocenter and represent an unusual class of indolines bearing structural resemblance to the hybrid natural product pleiocarpamine.

Mild, efficient Fischer indole synthesis using 2,4,6-trichloro-1,3,5- triazine (TCT)

Siddalingamurthy, Eranna,Mahadevan, Kittappa M.,Masagalli, Jagadeesh N.,Harishkumar, Hosanagara N.

supporting information, p. 5591 - 5596 (2013/09/23)

Mild and efficient protocol for the Fischer indole synthesis using TCT has been described. TCT serves as a mild and inexpensive catalyst. Under these conditions several functional groups such as ester, cyano, sulfone, amides, and ethers are tolerated. By this method, many functionalized analytically pure indoles were prepared easily without the need of purification.

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

What can I do for you?
Get Best Price

Get Best Price for 6722-06-1