Welcome to LookChem.com Sign In|Join Free
  • or
α-Dapiofuranosyl-1,2-cyclic phosphate is a chemical compound with the molecular formula C10H13N2O7P. It is derived from dapiofuranosyl, a modified sugar molecule, and features a cyclic phosphate group. α-dapiofuranosyl-1,2-cyclic phosphate is of interest in the field of chemistry, particularly in the study of nucleosides and their derivatives, as it represents a structural modification of a naturally occurring compound. The cyclic phosphate group imparts unique chemical properties to the molecule, which can be explored for potential applications in various chemical and biological processes.

30912-15-3

Post Buying Request

30912-15-3 Suppliers

Recommended suppliers

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

30912-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30912-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30912-15:
(7*3)+(6*0)+(5*9)+(4*1)+(3*2)+(2*1)+(1*5)=83
83 % 10 = 3
So 30912-15-3 is a valid CAS Registry Number.

30912-15-3Downstream Products

30912-15-3Relevant academic research and scientific papers

Isotope Probing of the UDP-Apiose/UDP-Xylose Synthase Reaction: Evidence of a Mechanism via a Coupled Oxidation and Aldol Cleavage

Eixelsberger, Thomas,Horvat, Doroteja,Gutmann, Alexander,Weber, Hansj?rg,Nidetzky, Bernd

, p. 2503 - 2507 (2017)

The C-branched sugar d-apiose (Api) is essential for plant cell-wall development. An enzyme-catalyzed decarboxylation/pyranoside ring-contraction reaction leads from UDP-α-d-glucuronic acid (UDP-GlcA) to the Api precursor UDP-α-d-apiose (UDP-Api). We examined the mechanism of UDP-Api/UDP-α-d-xylose synthase (UAXS) with site-selectively2H-labeled and deoxygenated substrates. The analogue UDP-2-deoxy-GlcA, which prevents C-2/C-3 aldol cleavage as the plausible initiating step of pyranoside-to-furanoside conversion, did not give the corresponding Api product. Kinetic isotope effects (KIEs) support an UAXS mechanism in which substrate oxidation by enzyme-NAD+and retro-aldol sugar ring-opening occur coupled in a single rate-limiting step leading to decarboxylation. Rearrangement and ring-contracting aldol addition in an open-chain intermediate then give the UDP-Api aldehyde, which is intercepted via reduction by enzyme-NADH.

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 30912-15-3