Product Document Searching Made Easy by 2D Code! | TCI Chemistry News October 2025 | [TCIPracticalExample] Di-Cbz Guanidinylation of Amine... | Various analytical charts can be searched on each product detail page and Product Document Search (The kinds of analytical charts differ by product)
Maximum quantity allowed is 999
Please select the quantity
CAS RN: 64443-05-6 | Product Number: T2665
Tetrakis(acetonitrile)copper(I) Hexafluorophosphate
×
![]()
×
Purity: >97.0%(T)
Synonyms:
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 5G |
NT$4,410
|
≥60 | 32 | It can be shipped in about 2 weeks after ordering |
* The above prices include freight cost, customs, and other charges to the destination except for products that need to be shipped by sea or dry ice. For details, please contact
our distributor
in Taiwan to order our product.
* The storage conditions are subject to change without notice.
| Product Number | T2665 |
Purity / Analysis Method 
|
>97.0%(T) |
| Molecular Formula / Molecular Weight | C__8H__1__2CuF__6N__4P = 372.72 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Frozen (<0°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive,Moisture Sensitive,Heat Sensitive |
| CAS RN | 64443-05-6 |
| Reaxys Registry Number | 14262634 |
| PubChem Substance ID | 87561580 |
| MDL Number | MFCD00064810 |
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(Potassium permanganate method) | min. 97.0 % |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 160 °C(dec.) |
GHS
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
| Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
| H.S.code* | 2931.59-000 |
Application
Perfluoroalkylation using Perfluoro Acid Anhydrides
Reference
- Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source
Application
Copper Catalyzed Asymmetric Conjugate Addition
References
- Catalytic Asymmetric Synthesis of Chiral Tertiary Organoboronic Esters through Conjugate Boration of β-Substituted Cyclic Enones
- Searching for Practically Useful P-Chirogenic Phosphine Ligands
Application
Catalytic Asymmetric Vinylogous Conjugate Addition of Unsaturated Butyrolactones to α,β-Unsaturated Thioamides
Reference
Application
Copper-catalyzed C―H Amidation of Unactivated Arenes
Typical Procedure:
To a stirred mixture of [Cu(CH3CN)4]PF6 (0.010 g, 0.026 mmol) and neocuproine (0.005 g, 0.024 mmol) in the arene (ca. 1 mL) is added N-tosyloxy-2,2,2-trichloroethylcarbamate (0.050 g, 0.138 mmol) and the mixture is allowed to stir at 140 °C for 8 h. The reaction mixture is cooled to room temperature, filtered through a pad of silica, washed with CH2Cl2, and the filtrate is concentrated under vacuum. The residue is purified by silica chromatography using 5–15% Et2O in hexanes to obtain the regioisomeric mixture of aminated arenes. The isomer ratio is determined by NMR using 1,3,5-trimethoxybenzene as a reference.
To a stirred mixture of [Cu(CH3CN)4]PF6 (0.010 g, 0.026 mmol) and neocuproine (0.005 g, 0.024 mmol) in the arene (ca. 1 mL) is added N-tosyloxy-2,2,2-trichloroethylcarbamate (0.050 g, 0.138 mmol) and the mixture is allowed to stir at 140 °C for 8 h. The reaction mixture is cooled to room temperature, filtered through a pad of silica, washed with CH2Cl2, and the filtrate is concentrated under vacuum. The residue is purified by silica chromatography using 5–15% Et2O in hexanes to obtain the regioisomeric mixture of aminated arenes. The isomer ratio is determined by NMR using 1,3,5-trimethoxybenzene as a reference.
References
PubMed Literature
Documents
Product Articles
[Research Articles] Perfluoroalkylation using Perfluoro Acid Anhydrides[Research Articles] Catalytic Asymmetric Vinylogous Conjugate Addition of Unsaturated Butyrolactones to α,β-Unsaturated Thioamides
[Research Articles] Copper-catalyzed C—H Amidation of Unactivated Arenes
Product Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
Please select Language.
The requested SDS is not available.
Please Contact Us for more information.
Specifications
C of A & Other Certificates
Please enter Lot Number
Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.
Sample C of A
This is a sample C of A and may not represent a recently manufactured lot of the product.
A sample C of A for this product is not available at this time.
Analytical Charts
Please enter Lot Number
Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.
The requested analytical chart is not available. Sorry for the inconvenience.