Product Introduction
| 1,3-Bis(trifluoromethyl)-benzene Basic information |
| Product Name: | 1,3-Bis(trifluoromethyl)-benzene |
| Synonyms: | ALPHA,ALPHA,ALPHA,ALPHA',ALPHA',ALPHA'-HEXAFLUORO-M-XYLENE;A,A,A,A',A',A'-HEXAFLUORO-M-XYLENE;1,3-BIS(TRIFLUOROMETHYL)BENZENE;1,3-DI(TRIFLUOROMETHYL)BENZENE;alpha,alpha,alpha,beta,beta,beta-hexafluoro-m-xylene;1,3-TrifluoromethylBenzene;1,3-Bis(trifluoromethyl)benzene, 98+%;M-BIS(TRIFLUORO-METNY)BENZENE |
| CAS: | 402-31-3 |
| MF: | C8H4F6 |
| MW: | 214.11 |
| EINECS: | 206-939-4 |
| Product Categories: | Aromatic Hydrocarbons (substituted) & Derivatives;Benzene derivatives |
| Mol File: | 402-31-3.mol |
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| 1,3-Bis(trifluoromethyl)-benzene Chemical Properties |
| Melting point | -35°C |
| Boiling point | 116-116.3 °C(lit.) |
| density | 1.378 g/mL at 25 °C(lit.) |
| refractive index | n20/D 1.379(lit.) |
| Fp | 26 °C |
| storage temp. | Sealed in dry,2-8°C |
| form | clear liquid |
| Specific Gravity | 1.378 |
| color | Colorless to Light yellow to Light orange |
| Water Solubility | Insoluble in water. Soluble in alcohol, ether, benzene. |
| BRN | 2052589 |
| Dielectric constant | 5.9800000000000004 |
| InChIKey | SJBBXFLOLUTGCW-UHFFFAOYSA-N |
| LogP | 3.83 |
| CAS DataBase Reference | 402-31-3(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzene, 1,3-bis(trifluoromethyl)-(402-31-3) |
| EPA Substance Registry System | Benzene, 1,3-bis(trifluoromethyl)- (402-31-3) |
| Safety Information |
| Hazard Codes | Xi,F |
| Risk Statements | 10-36/37/38 |
| Safety Statements | 26-24/25 |
| RIDADR | UN 1993 3/PG 3 |
| WGK Germany | 3 |
| Hazard Note | Flammable |
| TSCA | T |
| HazardClass | 3 |
| PackingGroup | III |
| HS Code | 29039990 |
| MSDS Information |
| Provider | Language |
|---|---|
| 1,3-Di(trifluoromethyl)benzene | English |
| ACROS | English |
| SigmaAldrich | English |
| ALFA | English |
| 1,3-Bis(trifluoromethyl)-benzene Usage And Synthesis |
| Chemical Properties | CLEAR COLOURLESS LIQUID |
| Uses | 1,3-Bis(trifluoromethyl)benzene undergoes regioselective metalation and subsequent carboxylation at position 2 to give 2,6-bis(trifluoromethyl)benzoic acid. a convenient, selective synthesis of bis[2,4-bis(trifluoromethyl)phenyl]phosphane derivatives with 1,3-bis(trifluoromethyl)benzene as starting material. |
| General Description | Lithiation reaction of 1,3-bis(trifluoromethyl)benzene has been investigated. 1,3-Bis(trifluoromethyl)benzene undergoes regioselective metalation and subsequent carboxylation at position 2 to give 2,6-bis(trifluoromethyl)benzoic acid. |
| 1,3-Bis(trifluoromethyl)-benzene Preparation Products And Raw materials |
| Raw materials | Hydrogen fluoride-->m-Xylene-->p-Fluorotoluene |
| Preparation Products | 3,5-Bis(trifluoromethyl)benzoic acid-->PERFLUORO-1,3-DIMETHYLCYCLOHEXANE-->PERFLUORO(METHYLCYCLOHEXANE)-->2,4-BIS(TRIFLUOROMETHYL)BENZOIC ACID-->3,5-Bis(trifluoromethyl)nitrobenzene-->3,5-Bis(trifluoromethyl)phenol-->3-METHYLBENZOTRIFLUORIDE-->Benzotrifluoride-->Isophthalic acid-->Benzenemethanol, 2,6-bis(trifluoromethyl)- |
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