Welcome to LookChem.com Sign In|Join Free
  • or
(1S,5R,6R,7S)-3,8-Dioxa-tricyclo[3.2.1.0^2,4^]octane-6,7-dicarboxylic acid is a complex organic compound with a unique cyclic structure. It features a tricyclic ring system with a 3,8-dioxa bridge, which means it has two oxygen atoms forming part of the ring. The compound has two carboxylic acid groups attached to the 6 and 7 positions of the ring, which are crucial for its reactivity and potential applications. The stereochemistry of the compound is defined by the (1S,5R,6R,7S) configuration, indicating the specific arrangement of atoms in three-dimensional space. (1S,5R,6R,7S)-3,8-Dioxa-tricyclo[3.2.1.02,4]octane-6,7-dicarboxylic acid is known for its potential use in the synthesis of various pharmaceuticals and other chemical products due to its rigid and functionalized structure.

18700-59-9

Post Buying Request

18700-59-9 Suppliers

Recommended suppliers

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

18700-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18700-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,0 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18700-59:
(7*1)+(6*8)+(5*7)+(4*0)+(3*0)+(2*5)+(1*9)=109
109 % 10 = 9
So 18700-59-9 is a valid CAS Registry Number.

18700-59-9Relevant academic research and scientific papers

CHEMICAL REPERCUSSIONS OF ORBITAL INTERACTIONS THROUGH BOND AND THROUGH SPACE. EFFECT OF REMOTE SUBSTITUENTS ON THE ADDITION OF NITRENES TO BICYCLIC OLEFINS

Aitken, R. Alan,Gosney, Ian,Farries, Hugh,Palmer, Michael H.,Simpson, Isobel,et. al.

, p. 1329 - 1346 (2007/10/02)

The reactivity of a series of bicyclic olefins with nitrenes is profoundly influenced by the nature of remote functional groups.There is a marked lack of reactivity for reactions with carboethoxynitrene as compared to phthalimidonitrene which is distinctly nucleophilic in character.An explanation for the reluctance to form aziridines is offered in terms of orbital interactions between the distant groups and the olefinic bond, making the latter remarkably electron deficient as evidenced by UV-photoelectron spectroscopy.Because of the complexity of the spectra, identification of the Ip associated with the reactive ?-centre was made by recourse to ab initio configuration interaction calculations for key members of the series.

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 18700-59-9