Welcome to LookChem.com Sign In|Join Free
  • or
ethyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

168644-99-3

Post Buying Request

168644-99-3 Suppliers

Recommended suppliers

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

168644-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168644-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,6,4 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168644-99:
(8*1)+(7*6)+(6*8)+(5*6)+(4*4)+(3*4)+(2*9)+(1*9)=183
183 % 10 = 3
So 168644-99-3 is a valid CAS Registry Number.

168644-99-3Downstream Products

168644-99-3Relevant academic research and scientific papers

Synthesis of analogues of calicheamicin and neocarzinostatin chromophore

Cirla, Alessandra,McHale, Angela R.,Mann, John

, p. 4019 - 4029 (2007/10/03)

The work presents a synthetic route to the CD ring of calicheamicin and in the case of neocarzinostatin an approach to a functionalised cyclopentane-1,3-diol containing the naturally occurring naphthoate and a glucosamine motif. In the case of the NCS derivative some biological activity (cytotoxicity) was observed.

New effective synthesis of (N-acetyl- and N-stearoyl-2-amino-2-deoxy-β-D-glucopyranosyl)-(1→4)N-acetyln or-muramoyl-L-2-aminobutanoyl-D-isoglutamine, analogs of GMDP with immunopotentiating activity

Ledvina, Miroslav,Zyka, Daniel,Jezek, Jan,Trnka, Tomas,Saman, David

, p. 577 - 589 (2007/10/03)

Ethyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (5), prepared by benzylation of ethyl 2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (4), was transformed by reaction with bromine into 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-

Synthesis of fully and partially benzylated glycosyl azides via thioalkyl glycosides as precursors for the preparation of N-glycopeptides

Kerekgyarto, Janos,Agoston, Karoly,Batta, Gyula,Kamerling, Johannis P.,Vliegenthart, Johannes F. G.

, p. 7189 - 7192 (2007/10/03)

Fully O-benzylated mono-, di- and trisaccharide glycosyl azides representing the reducing terminal of the core structure of N-glycans were synthesized. Totally and partially benzylated thioalkyl glucosamine glycosides were converted into the corresponding

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 168644-99-3