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5-bromo-1-(5-deoxy-5-fluoro-beta-L-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38817-30-0

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38817-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38817-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,1 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38817-30:
(7*3)+(6*8)+(5*8)+(4*1)+(3*7)+(2*3)+(1*0)=140
140 % 10 = 0
So 38817-30-0 is a valid CAS Registry Number.

38817-30-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-1-[(2S,3S,4R,5R)-5-(fluoromethyl)-3,4-dihydroxyoxolan-2-yl]pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Brom-5'-desoxy-5'-fluor-uridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38817-30-0 SDS

38817-30-0Upstream product

38817-30-0Relevant academic research and scientific papers

Fluorinase-coupled base swaps: Synthesis of [18F]-5′- deoxy-5′-fluorouridines

Winkler, Margit,Domarkas, Juozas,Schweiger, Lutz F.,O'Hagan, David

supporting information; experimental part, p. 10141 - 10143 (2009/05/30)

(Chemical Equation Presented) Making F-ases: One-pot fluorination/base-swap biotransformations were developed by coupling the fluorinase enzyme to nucleoside phosphorylases to generate 5′-deoxy-5′-fluoronucleosides (FDAs). These biotransformations are amenable to radiolabeling syntheses starting from [18F]fluoride ion, as exemplified by the synthesis of [18F]-5′-deoxy-5′-fluorouridines (see scheme), and demonstrate a new application of fluorinase as a catalyst for 18F-C bond formation.

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