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6,8-diethyl-2-hydroxymethyltetrahydrooxazolo(3,2-c)pyrimidine-5,7-(4H,6H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58137-53-4

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58137-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58137-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,3 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58137-53:
(7*5)+(6*8)+(5*1)+(4*3)+(3*7)+(2*5)+(1*3)=134
134 % 10 = 4
So 58137-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O4/c1-3-8-9(15)12(4-2)11(16)13-5-7(6-14)17-10(8)13/h7,14H,3-6H2,1-2H3

58137-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8-diethyl-2-(hydroxymethyl)-2,3-dihydro-[1,3]oxazolo[3,2-c]pyrimidine-5,7-dione

1.2 Other means of identification

Product number -
Other names Dhtopd

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:58137-53-4 SDS

58137-53-4Downstream Products

58137-53-4Relevant academic research and scientific papers

2-14C-1-Allyl-3,5-diethyl-6-chlorouracil II: Isolation and structures of the major sulfur-free and three minor sulfur-containing metabolites and mechanism of biotransformation.

Kaul,Hempel,Kiefer

, p. 897 - 900 (1982)

The metabolites of 1-allyl-3,5-diethyl-6-chlorouracil in rabbit urine were isolated by preparative thick-layer, liquid-column, and gas chromatography. With the aid of mass and 1H-NMR spectra, and by comparison with an authentic sample, the major metabolite, 1, was identified as 6,8-diethyl-2-hydroxymethyl-tetrahydrooxazolo-[3,2-c]-pyrimidine-5,7(4H,6H)-dione, Metabolite 2 as 1-allyl-3-ethyl-5-(1-hydroxyethyl)-6-methylthiouracil, Metabolite 3 as 1-allyl-3,5-diethyl-6-methylthiouracil, and Metabolite 4 as 6,8-diethyl-2-hydroxymethyl-tetrahydrothiazolo-[3,2-c]pyrimidine-5,7(4H,6H)-dione. The mechanism of the formation of sulfur-containing metabolites is discussed, and a new metabolic pathway for the formation of methylthio compounds is proposed.

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