Welcome to LookChem.com Sign In|Join Free
  • or
(1R,2S,5S,6R)-3-aza-3-benzyl-6-methoxycarbonylbicyclo<3.1.0>hexyl-2-methanol is a bicyclic compound with a bicyclo[3.1.0]hexane backbone, featuring a benzyl group, a methoxycarbonyl group, and a hydroxyl group attached to the bicyclic structure. The aza moiety, a nitrogen atom replacing a carbon atom in the ring, adds to its unique structure. The stereochemistry is specified by the (1R,2S,5S,6R) designation, which indicates the arrangement of the substituents around the bicyclic structure.

220623-23-4

Post Buying Request

220623-23-4 Suppliers

Recommended suppliers

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

220623-23-4 Usage

Uses

Used in Medicinal Chemistry:
(1R,2S,5S,6R)-3-aza-3-benzyl-6-methoxycarbonylbicyclo<3.1.0>hexyl-2-methanol is used as a potential candidate in medicinal chemistry due to its unique structure and functional groups, which may offer novel interactions with biological targets and contribute to the development of new pharmaceuticals.
Used in Organic Synthesis:
In the field of organic synthesis, (1R,2S,5S,6R)-3-aza-3-benzyl-6-methoxycarbonylbicyclo<3.1.0>hexyl-2-methanol can be utilized as a building block or intermediate for the synthesis of more complex organic molecules. Its specific stereochemistry and functional groups make it a valuable component in creating a variety of organic compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 220623-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,6,2 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220623-23:
(8*2)+(7*2)+(6*0)+(5*6)+(4*2)+(3*3)+(2*2)+(1*3)=84
84 % 10 = 4
So 220623-23-4 is a valid CAS Registry Number.

220623-23-4Relevant academic research and scientific papers

Cyclopropanation reactions of pyroglutamic acid-derived synthons with akylidene transfer reagents

Zhang, Rui,Mamai, Ahmed,Madalengoitia, Jose S.

, p. 547 - 555 (2007/10/03)

The cyclopropanation of unsaturated lactams 1 and 3 derived from pyroglutamic acid with nucleophilic alkylidene transfer reagents is investigated. Good-to-modest yields of cyclopropanes were obtained with most sulfur ylides explored. Syn/anti selectivity was found to be dependent on the synthon as well as the sulfur ylide. This cyclopropanation methodology is used in the synthesis of arginine and glutamic acid analogues.

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 220623-23-4