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244546

Sigma-Aldrich

Azidomethyl phenyl sulfide

95%

Synonym(s):

Phenylthiomethyl azide

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About This Item

Linear Formula:
C6H5SCH2N3
CAS Number:
77422-70-9
Molecular Weight:
165.22
MDL number:
MFCD00009700
UNSPSC Code:
12352100
PubChem Substance ID:
24854683
NACRES:
NA.22

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

244546-1G:
244546-10G:
244546-BULK:
244546-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BGBC2402V
BGBB1514V
05627BH
12308TZ
09520PO

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Anna Gorelik et al.
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)
Radek Liboska et al.
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
Atif Sarwar et al.
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
Daniel Zewge et al.
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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