- 4-BROMOTHIOPHENOL
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- $0.00 / 1KG
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2026-03-20
- CAS:106-53-6
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 20 mt
- 4-Bromothiophenol
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- $0.10 / 1KG
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2025-12-24
- CAS:106-53-6
- Min. Order: 1KG
- Purity: 99.0%
- Supply Ability: 1000 tons
- 4-Bromothiophenol
-
- $0.00 / 1kg
-
2025-06-20
- CAS:106-53-6
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 20tons
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| | 4-Bromothiophenol Basic information |
| | 4-Bromothiophenol Chemical Properties |
| Melting point | 73-76 °C (lit.) | | Boiling point | 239 °C (lit.) | | density | 1.5260 | | Fp | 239°C | | storage temp. | Inert atmosphere,Room Temperature | | Water Solubility | Slightly soluble in water | | pka | 6.08±0.10(Predicted) | | form | Crystals or Crystalline Powder | | color | White to beige | | Sensitive | Air Sensitive | | BRN | 507031 | | InChI | 1S/C6H5BrS/c7-5-1-3-6(8)4-2-5/h1-4,8H | | InChIKey | FTBCOQFMQSTCQQ-UHFFFAOYSA-N | | SMILES | Sc1ccc(Br)cc1 | | CAS DataBase Reference | 106-53-6(CAS DataBase Reference) | | NIST Chemistry Reference | Benzenethiol, 4-bromo-(106-53-6) | | EPA Substance Registry System | Benzenethiol, 4-bromo- (106-53-6) |
| Hazard Codes | Xi,T,C | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | RIDADR | 2923 | | WGK Germany | 3 | | F | 10-13-23 | | Hazard Note | Irritant | | TSCA | TSCA listed | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29309070 | | Storage Class | 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | | Hazard Classifications | Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 4-Bromothiophenol Usage And Synthesis |
| Chemical Properties | White to beige Crystalline powder or crystals, slightly soluble in water. Air sensitive, strongly irritating to eyes, respiratory system and skin. | | Uses | 4-Bromothiophenol is a reagent used in the synthesis of indolyl-3-ehtanone-α-thioethers which act as non-toxic antimalrial agents. These compounds show anti-malarial activity, with no toxicity to a HeLa cell line. | | Application | 4-Bromobenzenethiol can undergo Suzuki-Miyaura reaction on palladium nanoparticles, whereas on gold nanoparticles it only undergoes a self-coupling reaction, and these two processes are known as hot carrier-induced processes. | | Synthesis | 4-Bromothiophenol can be synthesized via the reduction of 4-bromo-benzenesulfonyl chloride by red phosphorus and iodine in an acidic solution. Hydrogenation of 4,4'-dibromodiphenyl disulfide also produces 4-bromothiophenol. |
| | 4-Bromothiophenol Preparation Products And Raw materials |
| Raw materials | 4-Bromobenzenesulfonyl chloride-->Phosphorus-->iodine-->4,4'-Dibromodiphenyl disulfide-->BIS(4-BROMOPHENYL)DISULFIDE | | Preparation Products | 4H-AMINO-6-BROMO-2,3-DIHYDROTHIOCHROMEN-1,1-DIOXIDE-->1-BENZOTHIOPHENE-5-CARBOXYLIC ACID-->4-Hydroxy-6-bromo-2,3-dihydrothiochromen-1,1-dioxide-->2-(1-BENZOTHIOPHEN-5-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE-->1-BROMO-4-(METHYLSULPHONYL)-2-NITROBENZENE-->(5-BROMO-3-BENZO[B]THIENYL)METHANOL-->1-BENZOTHIOPHENE-5-CARBONITRILE-->5-BROMOBENZO[B]THIOPHENE-3-CARBOXYLIC ACID-->BENZO[B]THIOPHEN-5-YL-5-BORONIC ACID-->6-bromo-2,3-dihydrothiochromen-1,1-dioxide-4-one-->5-Bromobenzo[c]thiophene-->1-(5-BROMO-1-BENZOTHIEN-3-YL)ETHANONE-->4-BROMOBENZENESULFONIC ACID MONOHYDRATE-->6-bromo-2,3-dihydrothiochromen-4-one-->4-Mercaptophenylboronic acid-->4-(ETHYLTHIO)BENZENEBORONIC ACID-->4-(Methylthio)phenylboronic acid-->4-(TRIFLUOROMETHYLTHIO)BROMOBENZENE-->1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) 2-methyl ester, (2R,4R)-rel--->4-[(4-BROMOPHENYL)SULFONYL]PIPERIDINE |
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