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13239-96-8

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13239-96-8 Usage

Uses

2,4-Dithiouridine (cas# 13239-96-8) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 13239-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13239-96:
(7*1)+(6*3)+(5*2)+(4*3)+(3*9)+(2*9)+(1*6)=98
98 % 10 = 8
So 13239-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O4S2/c12-3-4-6(13)7(14)8(15-4)11-2-1-5(16)10-9(11)17/h1-2,4,6-8,12-14H,3H2,(H,10,16,17)/t4-,6+,7?,8-/m1/s1

13239-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dithione

1.2 Other means of identification

Product number -
Other names Uridine,2,4-dithio

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:13239-96-8 SDS

13239-96-8Downstream Products

13239-96-8Relevant articles and documents

Synthesis and potency of novel uracil nucleotides and derivatives as P2Y2 and P2Y6 receptor agonists

Ko, Hyojin,Carter, Rhonda L.,Cosyn, Liesbet,Petrelli, Riccardo,de Castro, Sonia,Besada, Pedro,Zhou, Yixing,Cappellacci, Loredana,Franchetti, Palmarisa,Grifantini, Mario,Van Calenbergh, Serge,Harden, T. Kendall,Jacobson, Kenneth A.

, p. 6319 - 6332 (2008/12/21)

The phosphate, uracil, and ribose moieties of uracil nucleotides were varied structurally for evaluation of agonist activity at the human P2Y2, P2Y4, and P2Y6 receptors. The 2-thio modification, found previously to enhance P2Y2 receptor potency, could be combined with other favorable modifications to produce novel molecules that exhibit high potencies and receptor selectivities. Phosphonomethylene bridges introduced for stability in analogues of UDP, UTP, and uracil dinucleotides markedly reduced potency. Truncation of dinucleotide agonists of the P2Y2 receptor, in the form of Up4-sugars, indicated that a terminal uracil ring is not essential for moderate potency at this receptor and that specific SAR patterns are observed at this distal end of the molecule. Key compounds reported in this study include 9, α,β-methylene-UDP, a P2Y6 receptor agonist; 30, Up4-phenyl ester and 34, Up4-[1]glucose, selective P2Y2 receptor agonists; dihalomethylene phosphonate analogues 16 and 41, selective P2Y2 receptor agonists; 43, the 2-thio analogue of INS37217 (P1-(uridine-5′)-P4-(2′-deoxycytidine- 5′)tetraphosphate), a potent and selective P2Y2 receptor agonist.

Synthesis of 2,4-dithiouridine and 2-thiocytidine.

Ueda,Iida,Ikeda,Mizuno

, p. 666 - 667 (2007/10/08)

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