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696-06-0

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696-06-0 Usage

Chemical Properties

White Solid

Uses

A metabolite of 5-Fluorouracil. (F596000)

Synthesis Reference(s)

The Journal of Organic Chemistry, 72, p. 8573, 2007 DOI: 10.1021/jo071255z

Check Digit Verification of cas no

The CAS Registry Mumber 696-06-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 696-06:
(5*6)+(4*9)+(3*6)+(2*0)+(1*6)=90
90 % 10 = 0
So 696-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H5FN2O2/c5-2-1-6-4(9)7-3(2)8/h2H,1H2,(H2,6,7,8,9)

696-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoro-1,3-diazinane-2,4-dione

1.2 Other means of identification

Product number -
Other names 5,6-Dihydro-5-fluorouracil

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:696-06-0 SDS

696-06-0Upstream product

696-06-0Downstream Products

696-06-0Relevant articles and documents

Improved chemical syntheses of 5,6-dihydro-5-fluorouracil

LaFrate, Andrew L.,Katzenellenbogen, John A.

, p. 8573 - 8576 (2008/02/13)

(Chemical Equation Presented) 5,6-Dihydro-5-fluorouracil (5-DHFU) is a metabolite of the chemotherapy drug 5-fluorouracil (5-FU) of importance for biological studies. 5-DHFU has been prepared by enzymatic reduction of 5-FU and in very low yield by hydrogenation of 5-FU; however, a practical chemical synthesis is not available. Facile racemic syntheses of 5-DHFU from 5-FU or uracil, using p-methoxybenzyl protecting groups followed by L-Selectride reduction, are reported.

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