- 3-Methoxybenzenethiol
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- $0.00 / 1KG
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2026-01-30
- CAS:15570-12-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 20 mt
- 3-Methoxybenzenethiol
-
- $0.00 / 1KG
-
2025-06-27
- CAS:15570-12-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500000kg
- 3-Methoxybenzenethiol
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- $75.00 / 1kg
-
2025-06-03
- CAS:15570-12-4
- Min. Order: 10kg
- Purity: 0.99
- Supply Ability: 20tons
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| | 3-Methoxybenzenethiol Basic information |
| | 3-Methoxybenzenethiol Chemical Properties |
| Melting point | 264.4-268.3 °C (decomp) | | Boiling point | 223-226 °C (lit.) | | density | 1.13 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.587(lit.) | | Fp | 205 °F | | storage temp. | 2-8°C | | pka | 6.36±0.10(Predicted) | | form | clear liquid | | color | Colorless to Almost colorless | | Specific Gravity | 1.130 | | Water Solubility | Not miscible or difficult to mix in water. Soluble in methanol, benzene, hexane, toluene and dichloromethane. | | Sensitive | Stench | | BRN | 2041496 | | InChI | 1S/C7H8OS/c1-8-6-3-2-4-7(9)5-6/h2-5,9H,1H3 | | InChIKey | QMVAZEHZOPDGHA-UHFFFAOYSA-N | | SMILES | COc1cccc(S)c1 | | LogP | 2.320 (est) | | CAS DataBase Reference | 15570-12-4(CAS DataBase Reference) | | NIST Chemistry Reference | meta-Methoxybenzenethiol(15570-12-4) | | EPA Substance Registry System | Benzenethiol, 3-methoxy- (15570-12-4) |
| Hazard Codes | Xn,Xi | | Risk Statements | 20/21/22-36/37/38-22 | | Safety Statements | 26-36/37-37/39 | | RIDADR | UN 2810 6.1/PG 3 | | WGK Germany | 3 | | F | 13 | | Hazard Note | Harmful/Stench | | HazardClass | IRRITANT, STENCH | | PackingGroup | III | | HS Code | 29309070 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 3-Methoxybenzenethiol Usage And Synthesis |
| Chemical Properties | clear colorless to light yellow liquid | | Uses | Labelled analogue 3-Methoxy
cy as phencyclidine but differs in terms binding affinity. 3-Methoxy | | Uses | 3-Methoxythiophenol is used in the preparation of allenes. | | Synthesis | Taking m-bromoanisole as raw material, the organic magnesium compounds were firstly produced, then the Grignard reaction was carried out with solid sulfur, and finally 3-methoxybenzenethiol was produced by hydrolysis. The method is less polluting and easy to operate, with 51% total yield and 98% purity. |
| | 3-Methoxybenzenethiol Preparation Products And Raw materials |
| Raw materials | Carbamothioic acid, N,N-dimethyl-, S-(3-methoxyphenyl) ester-->Carbamothioic acid, N,N-dimethyl-, O-(3-methoxyphenyl) ester-->Disulfide, ethyl 3-methoxyphenyl (9CI)-->3-Methoxy-phenylthioaceticacid-->3-METHOXY THIOANISOLE-->3-Iodoanisole | | Preparation Products | Azuleno[4,5-b]furan-2,8(3H,4H)-dione,octahydro-4-hydroxy-9-methyl-3,6-bis(methylene)-, (3aR,4S,6aR,9S,9aR,9bR)--->4-METHOXYBENZENETHIOL-->2-(4-Hydroxyphenyl)benzo[b]thiophene-6-ol-->Benzo[b]thiophene-2-sulfonamide, 4-hydroxy--->Benzo[b]thiophene, 4-methoxy-3-methyl- |
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