Category: 274-78-2

Khan, Abdul Hakim published the artcileElectronic structure and spectra of indolizine and its aza derivatives, SDS of cas: 274-78-2, the main research area is PPP indolizine azaindolizine diazaindolizine electronic structure.

Indolizine and its aza derivatives were studied theor. using the method of Pariser, Parr and Pople modified by Dewar and Harget. The ground-state properties such as bond length, charge d., reactivity and π-dipole moment and other properties such as ionization potential, electron affinity, half-wave reduction potential and π* ← π spectra were predicted and correlated with the exptl. results where available.

Journal of the Indian Chemical Society published new progress about Atomization enthalpy. 274-78-2 belongs to class imidazoles-derivatives, name is Imidazo[1,2-c]pyrimidine, and the molecular formula is C6H5N3, SDS of cas: 274-78-2.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Evleth, Earl M. published the artcileSystematics of the electronic absorption spectra of fused 5-6 ring heterocyclics, HPLC of Formula: 274-78-2, the main research area is heterocyclics electronic spectra; electronic spectra heterocyclics; aza substitution spectral effect; indolizines spectra.

The electronic absorption spectra of indene, indole, benzofuran isoindole, indolizine, and 1- and 2-pyrindine are rationalized by using semiempirical SCF-configuration interaction calculations The absorption spectra of these materials are also rationalized by using indenyl anion as the common perturbational model. Perturbation theory is also applied to explaining the effect of aza-substitution on the spectra of indolizines.

Theoretica Chimica Acta published new progress about Heterocyclic compounds Role: PRP (Properties). 274-78-2 belongs to class imidazoles-derivatives, name is Imidazo[1,2-c]pyrimidine, and the molecular formula is C6H5N3, HPLC of Formula: 274-78-2.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Hall, Janet A. published the artcileThe induction of errors during in vitro DNA synthesis following chloroacetaldehyde-treatment of poly(dA-dT) and poly(dC-dG) templates, Application In Synthesis of 274-78-2, the main research area is chloroacetaldehyde DNA polymer reaction; polymerase DNA chloroacetaldehyde; ethenoadenine chloroacetaldehyde DNA; ethenocytosine chloroacetaldehyde DNA.

Chloroacetaldehyde [107-20-0], a rearranged metabolic product of the human carcinogen vinyl chloride, reacts with the DNA-like polymers poly(dA-dT) [26966-61-0] and poly(dC-dG) [62081-33-8] to form etheno-adducts of the adenine and cytosine bases. These treated polymers, when used as templates for Escherichia coli DNA polymerase I [9012-90-2] in an in vitro assay, show a decreased ability to direct DNA synthesis. At the same time, increased relative levels of noncomplementary nucleotides are incorporated. With the poly(dA-dT) templates, 1 dGMP residue is incorporated for every ∼60 ethenoadenine [13875-63-3] residues present, whereas no increased misincorporation of dCMP was detected. With the poly(dC-dG) templates, 1 misincorporation of dAMP or dTMP occurred in the presence of ∼30 and 80 ethenocytosine [274-78-2] residues, resp. A nearest neighbor anal. shows that with the modified poly(dC-dG) templates, the majority of the errors were incorporated opposite cytosine (or modified cytosine) bases.

Carcinogenesis published new progress about DNA Role: BIOL (Biological Study). 274-78-2 belongs to class imidazoles-derivatives, name is Imidazo[1,2-c]pyrimidine, and the molecular formula is C6H5N3, Application In Synthesis of 274-78-2.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem