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127527-24-6

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127527-24-6 Usage

General Description

2,5-Pyrimidinedicarboxylic acid (9CI) is a chemical compound with the molecular formula C6H4N2O4. It is a type of pyrimidine derivative and an isomer of uracil, which is a component of RNA. 2,5-Pyrimidinedicarboxylicacid(9CI) has two carboxylic acid functional groups, which can make it a useful building block for the synthesis of various organic compounds. It has potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique molecular structure and properties. Additionally, 2,5-Pyrimidinedicarboxylic acid (9CI) is also used as a precursor in the production of various dyes, pigments, and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 127527-24-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,2 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127527-24:
(8*1)+(7*2)+(6*7)+(5*5)+(4*2)+(3*7)+(2*2)+(1*4)=126
126 % 10 = 6
So 127527-24-6 is a valid CAS Registry Number.

127527-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrimidine-2,5-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2,5-pyrimidinecarboxylic acid

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:127527-24-6 SDS

127527-24-6Relevant articles and documents

New electron-transporting materials for light emittind diodes: 1,3,4-oxadiazole-pyridine and 1,3,4-oxadiazole-pyrimidine hybrids

Wang, Changsheng,Jung, Gun-Young,Batsanov, Andrei S.,Bryce, Martin R.,Petty, Michael C.

, p. 173 - 180 (2007/10/03)

We described the synthesis of three new isomeric 1,3,4-oxadiazole-pyridine hybrids, namely: 2,6-, 3,5- and 2,4-bis[2-(4-tert-butylphenyl)-1,3,4-oxadiazol-5-yl]pyridine, (PDPy-2,6, PDPy-3,5 and PDPy-2,4, respectively) and a 1,3,4-oxadiazole-pyrimidine hybrid, namely: 2,5-bis[2-(4-tert-butylphenyl)-1,3,4-oxadiazol-5-yl]pyrimidine (PDPmDP). The X-ray crystal structures are reported for PDPy-2,4 and the known phenylene analogue 1,3-bis[2-(4-tert-butylphenyl)-1,3,4-oxadiazol-5-yl]benzene (OXD-7) as a 1:1 toluene solvate. The packing motif for molecules of both PDPy-2,4 and OXD-7 is that of discrete layers with the mean planes of all the molecules in the crystals parallel to within 6 deg. We have fabricated light-emitting diodes (LEDs) using poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV) doped with rubrene as the emissive material, with and withuot a thermally evaporated electron conducting/hole blocking (ECHB) layer of PDPy-2,6, PDPy-3,5 and PDPy-2,4, PDPmDP and OXD-7, in the device configuration ITO/MEH-PPV(Ru)/ECHB layer/Al. Electroluminescence spectra indicate that light is emitted only from the MEH-PPV layer. The bilayer LEDs are considerably more efficient that single layer devices, e.g. the external quantum efficiences of devices incorporating PDPy-2,6, PDPy-3,5 and OXD-7 are 0.14, 0.04 and 0.06 percent at 40 mAm-2, respectively , cf. 0.007 percent for the reference single-layer MEH-PPV(Ru) device. There is no clear correlation between experomental EQE values and the PM3 calculated LUMO levels of the materials.

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