Welcome to LookChem.com Sign In|Join Free
  • or
Methyl 4,6-di-O-benzoyl-2,3-dideoxy-α-D-threo-hex-2-enopyranoside is a complex organic compound with the molecular formula C21H20O6. It is a derivative of a hexopyranoside, which is a type of sugar molecule. The compound features a methyl group attached to the 4,6-di-O-benzoyl-2,3-dideoxy-α-D-threo-hex-2-enopyranose structure. The benzoyl groups are ester derivatives of benzoic acid, which are attached to the 4th and 6th carbon atoms of the sugar ring. The dideoxy notation indicates that two hydroxyl groups are missing from the sugar molecule, and the α-D-threo configuration describes the spatial arrangement of the atoms in the molecule. methyl 4,6-di-O-benzoyl-2,3-dideoxy-α-D-threo-hex-2-enopyranoside is often used in the synthesis of complex carbohydrates and as an intermediate in the preparation of various pharmaceuticals and biologically active compounds.

6605-38-5

Post Buying Request

6605-38-5 Suppliers

Recommended suppliers

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

6605-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6605-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6605-38:
(6*6)+(5*6)+(4*0)+(3*5)+(2*3)+(1*8)=95
95 % 10 = 5
So 6605-38-5 is a valid CAS Registry Number.

6605-38-5Downstream Products

6605-38-5Relevant academic research and scientific papers

Selective Synthesis of Partially Protected d -Talopyranosides and d -Gulopyranosides via Catalytic Asymmetric Dihydroxylation: Multiplier Effects of Substrate Control and Catalyst Control

Namito, Yoichi,Michigami, Kyosuke,Nagahashi, Takaaki,Matsubara, Ryosuke,Hayashi, Masahiko

, p. 6058 - 6061 (2016)

Highly selective syntheses of d-talopyranosides and d-gulopyranosides have been achieved by utilizing the multiplier effects of substrate control and catalyst control. Through the combination of an O-benzoyl-protected substrate and the AD-mix-β system, the d-talopyranoside was obtained in a ratio of 96:4. In contrast, the d-gulopyranoside was obtained in a ratio of 3:97 through the use of an O-tert-butyldimethylsilyl-protected substrate and AD-mix-α.

Selective Synthesis of Some Aminosugars via Catalytic Aminohydroxylation of Protected 2,3-Unsaturated d -Gluco- And d -Galacto-2-hexenopyranosides

Fukuhara, Ippei,Matsubara, Ryosuke,Hayashi, Masahiko

, p. 9179 - 9189 (2020/08/14)

The aminohydroxylation of methyl 4,6-di-O-(tert-butyldimethylsilyl)-2,3-unsaturated α-d-glucopyranoside proceeds in the presence of chloramine-T, OsO4 (4 mol %), (DHQ)2PHAL (5 mol %), and triethylbenzylammonium chloride (TEBAC) in both a stereoselective a

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 6605-38-5