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Key Documents

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850187

Sigma-Aldrich

5-Bromouridine

98%

Sinónimos:

5-Bromouracil-1-β-D-ribofuranoside

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About This Item

Fórmula empírica (notación de Hill):
C9H11BrN2O6
Número de CAS:
957-75-5
Peso molecular:
323.10
Beilstein/REAXYS Number:
33664
EC Number:
213-486-6
MDL number:
MFCD00006528
UNSPSC Code:
12352204
PubChem Substance ID:
24888292
NACRES:
NA.22

Quality Level

100

assay

98%

form

crystals

optical activity

[α]22/D −11°, c = 2 in H2O

mp

180-182 °C (dec.) (lit.)

storage temp.

−20°C

SMILES string

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=C(Br)C(=O)NC2=O

InChI

1S/C9H11BrN2O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2H2,(H,11,16,17)/t4-,5-,6-,8-/m1/s1

InChI key

AGFIRQJZCNVMCW-UAKXSSHOSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Extensive gene expression during meiosis is a hallmark of spermatogenesis. Although it was generally accepted that RNA transcription ceases during meiosis, recent observations suggest that some transcription occurs in postmeiosis. To further resolve this issue, we provide direct evidence for
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Genome research, 22(5), 947-956 (2012-03-01)
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Nikolay A Grigorenko et al.
Chemical communications (Cambridge, England), (42)(42), 5417-5419 (2008-11-06)
Within an oligonucleotide duplex, excess electron transfer from a excited 5-(pyren-1-yl)uridine through an internal stacked phenanthrenyl pair to 5-bromouridine as an electron acceptor was observed.
Thomas Pesnot et al.
Organic & biomolecular chemistry, 6(16), 2884-2891 (2008-08-09)
A series of novel 5-substituted UDP-glucose derivatives with interesting fluorescent properties and potential applications as sensors for carbohydrate-active enzymes is reported. An efficient synthesis of the target molecules was developed, centred around the Suzuki-Miyaura reaction of (hetero)arylboronic acids with 5-iodo
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