244546
Azidomethyl phenyl sulfide
95%
Synonym(s):
Phenylthiomethyl azide
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About This Item
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Assay
95%
reaction suitability
reaction type: click chemistry
refractive index
n20/D 1.5904 (lit.)
bp
104-105 °C/5 mmHg (lit.)
density
1.168 g/mL at 25 °C (lit.)
functional group
azide
thioether
storage temp.
2-8°C
SMILES string
[N-]=[N+]=NCSc1ccccc1
InChI
1S/C7H7N3S/c8-10-9-6-11-7-4-2-1-3-5-7/h1-5H,6H2
InChI key
KIQGRMGPIMCXSC-UHFFFAOYSA-N
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
226.4 °F - closed cup
Flash Point(C)
108 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Frontiers in molecular neuroscience, 11, 150-150 (2018-06-06)
The complement system, which is part of the innate immune response system, has been recently shown to participate in multiple key processes in the developing brain. Here we aimed to elucidate downstream signaling responses linking complement C3, a key molecule
Versatile post-polymerization functionalization of poly (p-phenylene vinylene) copolymers containing carboxylic acid substituents: development of a universal method towards functional conjugated copolymers.
Polym. Chem., 1(8), 1313-1322 (2010)
PloS one, 7(12), e51679-e51679 (2012-12-29)
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
PloS one, 10(4), e0123084-e0123084 (2015-05-01)
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
Bioconjugate chemistry, 25(12), 2222-2232 (2014-11-15)
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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