Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121843-63-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 121843-63-8 Structure
  • Basic information

    1. Product Name: 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone
    2. Synonyms: 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone
    3. CAS NO:121843-63-8
    4. Molecular Formula:
    5. Molecular Weight: 565.666
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121843-63-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone(121843-63-8)
    11. EPA Substance Registry System: 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone(121843-63-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 121843-63-8(Hazardous Substances Data)

121843-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121843-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,4 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121843-63:
(8*1)+(7*2)+(6*1)+(5*8)+(4*4)+(3*3)+(2*6)+(1*3)=108
108 % 10 = 8
So 121843-63-8 is a valid CAS Registry Number.

121843-63-8Downstream Products

121843-63-8Relevant articles and documents

Optimized and Scalable Synthesis of Carba-α-d-Glucosamine

Babczyk, Alexander,Menche, Dirk,Wingen, Lukas M.

, p. 6645 - 6648 (2020)

An efficient, high-yielding synthesis of carba-α-d-glucosamine is reported. Key features of this optimized route include an innovative protecting group strategy and an unusual, stereoconvergent Ferrier carbocyclization of a hindered substrate. The sequenc

Fluoro-Carba-Sugars are Glycomimetic Activators of the glmS Ribozyme

Matzner, Daniel,Schüller, Anna,Seitz, Torben,Wittmann, Valentin,Mayer, Günter

, p. 12604 - 12612 (2017/09/18)

The glmS ribozyme is a bacterial gene-regulating riboswitch that controls cell wall synthesis, depending on glucosamine-6-phosphate as a cofactor. Due to the presence of this ribozyme in several human pathogen bacteria (e.g., MRSA, VRSA), the glmS ribozyme represents an attractive target for the development of artificial cofactors. The substitution of the ring oxygen in carbohydrates by functionalized methylene groups leads to a new generation of glycomimetics that exploits distinct interaction possibilities with their target structure in biological systems. Herein, we describe the synthesis of mono-fluoro-modified carba variants of α-d-glucosamine and β-l-idosamine. (5aR)-Fluoro-carba-α-d-glucosamine-6-phosphate is a synthetic mimic of the natural ligand of the glmS ribozyme and is capable of effectively addressing its unique self-cleavage mechanism. However, in contrast to what was expected, the activity is significantly decreased compared to its non-fluorinated analog. By combining self-cleavage assays with the Bacillus subtilis and Staphylococcus aureus glmS ribozyme and molecular docking studies, we provide a structure–activity relationship for fluorinated carba-sugars.

Synthesis of the carbon pseudosugar analog of lipid X

Miyamoto,Baker,Lewis

, p. 3725 - 3728 (2007/10/02)

A carbocyclic analog (2) with a deactivated pseudo-anomeric phosphate of the lipopolysaccharide biosynthetic intermediate Lipid X (1) was prepared in order to better understand the biological behavior of the parent compound. Two related synthetic routes t

SYNTHETIC METHODS FOR THE PREPARATION OF BASIC D- AND L-PSEUDO-SUGARS. SYNTHESIS OF CARBOCYCLIC ANALOGUES OF N-ACETYL-MURAMYL-L-ALANYL-D-ISOGLUTAMINE (MDP)

Barton, Derek H. R.,Augy-Dorey, S.,Camara, J.,Dalko, P.,Delaumeny, J. M.,et al.

, p. 215 - 230 (2007/10/02)

Two exocyclic olefins 10 and 22, readily elaborated from D-glucosamine, have been transformed by Ferrier rearrangement reaction into aminocyclohexanones 11, 12 and 23, 24.Reduction of ketone 11 with tri-t-butoxy-aluminium hydride followed by sequential ac

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 121843-63-8