Welcome to LookChem.com Sign In|Join Free
  • or
Octahydro-5,7-dimethylindolizine is a heterocyclic organic compound with the molecular formula C9H17N. It is a colorless liquid with a density of 0.91 g/cm3 and a boiling point of 206-207°C. Octahydro-5,7-dimethylindolizine is a derivative of indolizine, which is a bicyclic aromatic system consisting of a six-membered ring fused to a five-membered nitrogen-containing ring. The two methyl groups in the compound are attached to the 5th and 7th carbon atoms of the indolizine structure. Octahydro-5,7-dimethylindolizine is synthesized through various chemical reactions and is used in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the field of materials science, particularly in the development of new polymers and dyes.

6753-28-2

Post Buying Request

6753-28-2 Suppliers

Recommended suppliers

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

6753-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6753-28-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6753-28:
(6*6)+(5*7)+(4*5)+(3*3)+(2*2)+(1*8)=112
112 % 10 = 2
So 6753-28-2 is a valid CAS Registry Number.

6753-28-2Upstream product

6753-28-2Downstream Products

6753-28-2Relevant academic research and scientific papers

Stereocontrolled synthesis of substituted chiral piperidines viaone-pot asymmetric 6π-azaelectrocyclization: Asymmetric syntheses of(-)-dendroprimine, (+)-7-epidendroprimine, (+)-5-epidendroprimine, and (+)-5,7-epidendroprimine

Kobayashi, Toyoharu,Hasegawa, Futoshi,Hirose, Yoshikatsu,Tanaka, Katsunori,Mori, Hajime,Katsumura, Shigeo

, p. 1812 - 1832 (2012/04/04)

The asymmetric one-pot 6π-azaelectrocyclization of alkenyl vinyl stannane, ethyl (Z)-2-iodo-4-oxobutenoate, and (-)-7-isopropyl-cis-aminoindanol in the presence of a Pd(0) catalyst stereoselectively produced the tetracyclic aminoacetal compounds, resultin

Synthesis of 2,4,6-trisubstituted chiral piperidines and (-)-dendroprimine by one-pot asymmetric azaelectrocyclization protocol

Kobayashi, Toyoharu,Hasegawa, Futoshi,Tanaka, Katsunori,Katsumura, Shigeo

, p. 3813 - 3816 (2007/10/03)

Stereocontrolled synthesis of 2,4,6-trisubstituted piperidine diastereomers has been realized from common intermediates, obtained by a one-pot azaelectrocyclization protocol. Based on the method, the asymmetric synthesis of an indolizidine alkaloid, (-)-d

Enantioselective synthesis of (-)-dendroprimine and isomers

De Saboulin Bollena, Axelle,Gelas-Mialhe, Yvonne,Gramain, Jean-Claude,Perret, Anne,Remuson, Roland

, p. 1029 - 1031 (2007/10/03)

An enantioselective and diastereoselective synthesis of six 5,7-dimethylindolizidine isomers is described via an intramolecular cyclization that involves an allylsilyl nucleophilic group and an acyliminium ion. The first total synthesis of naturally occurring (-)-dendroprimine has been achieved in five steps.

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 6753-28-2