244546
Azidomethyl phenyl sulfide
95%
Sinônimo(s):
Phenylthiomethyl azide
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About This Item
Fórmula linear:
C6H5SCH2N3
Número CAS:
Peso molecular:
165.22
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
95%
adequação da reação
reaction type: click chemistry
índice de refração
n20/D 1.5904 (lit.)
p.e.
104-105 °C/5 mmHg (lit.)
densidade
1.168 g/mL at 25 °C (lit.)
grupo funcional
azide
thioether
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
[N-]=[N+]=NCSc1ccccc1
InChI
1S/C7H7N3S/c8-10-9-6-11-7-4-2-1-3-5-7/h1-5H,6H2
chave InChI
KIQGRMGPIMCXSC-UHFFFAOYSA-N
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
226.4 °F - closed cup
Ponto de fulgor (°C)
108 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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5-Bromo-2'-deoxyuridine (BrdU) and 2'-deoxy-5-ethynyluridine (EdU) are widely used as markers of replicated DNA. While BrdU is detected using antibodies, the click reaction typically with fluorescent azido-dyes is used for EdU localisation. We have performed an analysis of ten samples of
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Recently, the attention of researchers has been drawn toward the synthesis of chitosan derivatives and their nanoparticles with enhanced antimicrobial activities. In this study, chitosan derivatives with different azides and alkyne groups were synthesized using click chemistry, and these were
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Chemical modification of siRNA is achieved in a high-throughput manner (96-well plate format) by copper catalyzed azide-alkyne cycloadditions. This transformation can be performed in one synthetic operation at up to four positions with complete specificity, good yield, and acceptable purity.
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