Welcome to LookChem.com Sign In|Join Free
  • or
(2R,3R,4R,5R,6S)-2-(acetoxymethyl)-5-azido-6-((tert-butyldiphenylsilyl)oxy)tetrahydro-2H-pyran-3,4-diyl diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132183-14-3

Post Buying Request

132183-14-3 Suppliers

Recommended suppliers

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

132183-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132183-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,8 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132183-14:
(8*1)+(7*3)+(6*2)+(5*1)+(4*8)+(3*3)+(2*1)+(1*4)=93
93 % 10 = 3
So 132183-14-3 is a valid CAS Registry Number.

132183-14-3Downstream Products

132183-14-3Relevant academic research and scientific papers

A highly stereoselective synthesis of di- and trimeric sialosyltn epitope: A partial structure of glycophorin A

Nakahara, Yoshiaki,Iijima, Hiroyuki,Sibayama, Shohei,Ogawa, Tomoya

, p. 6897 - 6900 (1990)

Di- and trimeric sialosyl-Tn epitope, prototype molecules of O-linked (mucin type) sialoglycoproteins, were synthesized in a stereocontrolled manner.

One-Step TEMPO-Catalyzed and Water-Mediated Stereoselective Conversion of Glycals into 2-Azido-2-deoxysugars with a PIFA-Trimethylsilyl Azide Reagent System

Chennaiah, Ande,Vankar, Yashwant D.

supporting information, p. 2611 - 2614 (2018/05/17)

An unprecedented water-mediated and TEMPO-catalyzed, one-step, highly regiospecific and stereoselective functionalization of glycals to 2-azido-2-deoxysugars has been developed using a PIFA-Me3SiN3 reagent system in the presence of B

Synthesis of Tunicaminyluracil Derivatives

Ichikawa, Satoshi,Matsuda, Akira

, p. 239 - 253 (2007/10/03)

A tunicaminyluracil derivative, which is a key component of the tunicamycin nucleoside antibiotics, was synthesized using a samarium diiodide (Sml2) mediated aldol reaction and intramolecular Pummerer reaction as the key steps. The α-phenylthio

Stereoselective total synthesis of glycopeptides bearing the dimeric and trimeric sialosyl-Tn epitope

Nakahara, Yoshiaki,Iijima, Hiroyuki,Shibayama, Shohei,Ogawa, Tomoya

, p. 211 - 225 (2007/10/02)

The dimeric and trimeric sialosyl-Tn epitopes, 6)-α-D-GalpNAc-(1->3)-L-Ser>n-L-Val (n = 2 and 3), which represent part of a clustered carbohydrate region of glycophorin A, a human erythrocyte glycoprotein, have been synthesised

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 132183-14-3