4-Bromothiophenol

Modify Date: 2024-01-02 11:24:15

4-Bromothiophenol Structure
4-Bromothiophenol structure
Common Name 4-Bromothiophenol
CAS Number 106-53-6 Molecular Weight 189.073
Density 1.6±0.1 g/cm3 Boiling Point 231.3±13.0 °C at 760 mmHg
Molecular Formula C6H5BrS Melting Point 73-76 °C(lit.)
MSDS Chinese USA Flash Point 93.7±19.8 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 4-bromothiophenol
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Boiling Point 231.3±13.0 °C at 760 mmHg
Melting Point 73-76 °C(lit.)
Molecular Formula C6H5BrS
Molecular Weight 189.073
Flash Point 93.7±19.8 °C
Exact Mass 187.929520
PSA 38.80000
LogP 3.53
Vapour Pressure 0.1±0.4 mmHg at 25°C
Index of Refraction 1.631
Storage condition Refrigerator

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S26
RIDADR 2923
WGK Germany 3
Packaging Group III
Hazard Class 8
HS Code 29309070

 Synthetic Route

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles3

More Articles
Electrophilic properties of patulin. Adduct structures and reaction pathways with 4-bromothiophenol and other model nucleophiles.

Chem. Res. Toxicol. 13(5) , 363-72, (2000)

The mycotoxin patulin (PAT) is believed to exert its cytotoxic and chromosome-damaging effects by forming covalent adducts with essential cellular thiols. Since the chemical structures of such adducts...

Direct identification of on-bead peptides using surface-enhanced Raman spectroscopic barcoding system for high-throughput bioanalysis.

Sci. Rep. 5 , 10144, (2015)

Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinc...

Formation and reactivity of chromium(V)-thiolato complexes: a model for the intracellular reactions of carcinogenic chromium(VI) with biological thiols.

J. Am. Chem. Soc. 132(25) , 8720-31, (2010)

The nature of the long-lived EPR-active Cr(V) species observed in cells and biological fluids exposed to carcinogenic Cr(VI) has been definitively assigned from detailed kinetic and spectroscopic anal...

 Synonyms

4-Bromothiophenol
4-Bromobenzenethiol
MFCD00004845
Benzenethiol, 4-bromo-
Benzenethiol, p-bromo-
p-Bromothiophenol
EINECS 203-407-3
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