Welcome to LookChem.com Sign In|Join Free
  • or
4,5-di-O-acetyl-3,6-anhydro-L-lyxo-2-hexulose phenylosazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81823-52-1

Post Buying Request

81823-52-1 Suppliers

Recommended suppliers

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

81823-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81823-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,2 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81823-52:
(7*8)+(6*1)+(5*8)+(4*2)+(3*3)+(2*5)+(1*2)=131
131 % 10 = 1
So 81823-52-1 is a valid CAS Registry Number.

81823-52-1Downstream Products

81823-52-1Relevant academic research and scientific papers

STUDIES ON 3-EPIMERIC L-2-HEXULOSE PHENYLOSAZONES. STRUCTURE AND ANOMERIC CONFIGURATION OF THE 3,6-ANHYDRO-OSAZONE DERIVATIVES OBTAINED FROM L-xylo- AND L-lyxo-2-HEXULOSE PHENYLOSAZONE

Sallam, Mohammed A.E.,Hegazy, Estrwah I.A.,Whistler, Roy L.,Markley, John L.,Croll, David H.

, p. 197 - 206 (1982)

Dehydration of the 3-epimeric 2-hexulose phenylosazones L-xylo-hexulose phenylosazone and L-lyxo-hexulose phenylosazone afforded 3,6-anhydro-L-lyxo-2-hexulose phenylosazone (2) as the preponderant isomer from both.The identity of 2 was obtained by t.l.c., and by acetylation followed by comparison of the products.Acetylation of 2 with acetic anhydride-pyridine afforded the di-O-acetyl derivative 4, and further acetylation gave the N-acetyl-di-O-acetyl derivative 5.Refluxing of 2 with copper sulfate afforded a C-nucleoside analog, namely, 2-phenyl-4-α-L-threo-furanosyl-1,2,3-osotriazole (6).The anomeric configuration was determined by n.m.r. spectroscopy.The stereochemical course of the dehydration process and the mass spectra of compounds 2, 4, 5, and 6 are discussed.

STRUCTURE AND ANOMERIC CONFIGURATION OF THE 3,6-ANHYDRO-OSAZONE DERIVATIVES OBTAINED FROM D-lyxo-HEXULOSE PHENYLOSAZONE AND D-xylo-HEXULOSE PHENYLOSAZONE

Sallam, Mohammed A. E.,Hegazy, Estrwah I. A.

, p. 91 - 98 (2007/10/02)

Dehydration of D-lyxo-hexulose phenylosazone or D-xylo-hexulose phenylosazone afforded 3,6-anhydro-D-lyxo-hexulose phenylosazone (2) as the preponderant isomer from both.The identity of 2 was obtained by acetylation, and comparison of the products.Acetylation with acetic anhydride-pyridine afforded the same di-O-acetyl derivative, and further acetylation afforded the same N-acetyldi-O-acetyl derivative (5).Refluxing 2 with copper sulfate afforded a C-nucleoside analog, namely, 2-phenyl-4-α-D-threofuranosyl-1,2,3-osotriazole (6).The anomeric configuratin of 2, 5, and 6 was determined by n.m.r. spectroscopy.The mechanism of the dehydrative cyclization-process, and the conformational stability of 2, are discussed.

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 81823-52-1