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2,4-Difluorotoluene

99%

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About This Item

Fórmula linear:
CH3C6H3F2
Número CAS:
Peso molecular:
128.12
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

99%

Formulário

liquid

índice de refração

n20/D 1.449 (lit.)

p.e.

113-117 °C (lit.)

densidade

1.12 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

Cc1ccc(F)cc1F

InChI

1S/C7H6F2/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3

chave InChI

MPXDAIBTYWGBSL-UHFFFAOYSA-N

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Descrição geral

2,4-Difluorotoluene was synthesized as a nucleotide analog and was incorporated into DNA and undergoes replication by DNA polymerase enzymes[1].

Aplicação

2,4-Difluorotoluene was used in the synthesis of new hydrophobic isosteres of pyrimidines and purine nucleosides[2].

Pictogramas

Flame

Palavra indicadora

Danger

Frases de perigo

Declarações de precaução

Classificações de perigo

Flam. Liq. 2

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

59.0 °F - closed cup

Ponto de fulgor (°C)

15 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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B D Silverman et al.
Journal of biomolecular structure & dynamics, 16(6), 1169-1175 (1999-08-14)
Molecular moment descriptors of the shape and charge distributions of twenty five nucleoside structures have been examined. The structures include thymidine as well as the difluorotoluene nucleoside analog which has been found to pair efficiently with adenine by polymerase catalysis.
Adriana Irimia et al.
The Journal of biological chemistry, 282(50), 36421-36433 (2007-10-24)
The 2,4-difluorotoluene (DFT) analog of thymine has been used extensively to probe the relative importance of shape and hydrogen bonding for correct nucleotide insertion by DNA polymerases. As far as high fidelity (A-class) polymerases are concerned, shape is considered by
Pradeep S Pallan et al.
Journal of the American Chemical Society, 131(35), 12548-12549 (2009-08-19)
Certain DNA polymerases (pols) were found to efficiently insert A opposite the hydrophobic T isostere 2,4-difluorotoluene (F) and vice versa, resulting in the widely held belief that some pols rely on shape rather than H-bonding for accurate replication. Using X-ray
Shuangluo Xia et al.
Biochemistry, 51(7), 1476-1485 (2012-02-07)
We have recently challenged the widely held view that 2,4-difluorotoluene (dF) is a nonpolar isosteric analogue of the nucleotide dT, incapable of forming hydrogen bonds (HBs). To gain a further understanding for the kinetic preference that favors dAMP insertion opposite
J C Morales et al.
Biochemistry, 39(10), 2626-2632 (2000-03-08)
We describe studies aimed at evaluating the physical factors governing the rate of 3'-end proofreading by the Klenow fragment of E. coli DNA polymerase I. Two nonpolar deoxynucleoside isosteres containing 2,4-difluorotoluene (F) and 4-methylbenzimidazole (Z), which are non-hydrogen-bonding shape mimics

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