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Chemical plants supply high-quality TRIPHENYLCARBENIUM TETRAFLUOROBORATE 341-02-6 in bulk
- Molecular Formula: C19H15BF4
- Molecular Weight: 330.133
- Appearance/Colour: ochre-yellow to orange crystalline powder
- Melting Point: 205-215 °C (dec.)(lit.)
- PSA: 0.00000
- LogP: 6.00580
TRIPHENYLCARBENIUM TETRAFLUOROBORATE(Cas 341-02-6) Usage
InChI:InChI=1/C19H15.BF4/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;2-1(3,4)5/h1-15H;/q+1;-1
341-02-6 Relevant articles
Carbene-based lewis pairs for hydrogen activation
Runyon, Jason W.,Steinhof, Oliver,Dias, H. V. Rasika,Calabrese, Joseph C.,Marshall, William J.,Arduengo, Anthony J.
, p. 1165 - 1172 (2011)
A series of Lewis acidbase pairs contain...
Synthesis and structure of tritylium salts
Hinz, Alexander,Labbow, René,Rei?, Fabian,Schulz, Axel,Sievert, Katharina,Villinger, Alexander
, p. 1641 - 1650 (2015/10/28)
Several tritylium compounds [Ph3C][A] ha...
Optimized synthesis and detailed NMR spectroscopic characterization of the 1,8a-dihydroazulene-1,1-dicarbonitrile photoswitch
Broman, Soren Lindbaek,Brand, Sophie Lehn,Parker, Christian Richard,Petersen, Michael Axman,Tortzen, Christian Gregers,Kadziola, Anders,Kilsa, Kristine,Nielsen, Mogens Brondsted
experimental part, p. 51 - 67 (2011/06/19)
An economical and effective protocol for...
Synthesis and Isolation of Polytrityl Cations by Utilizing Hexaphenylbenzene and Tetraphenylmethane Scaffolds
Rathore, Rajendra,Burns, Carrie L.,Guzei, Ilia A.
, p. 1524 - 1530 (2007/10/03)
The successful isolation of stable (and ...
341-02-6 Process route
-
-
76-84-6
triphenylmethyl alcohol
-
-
341-02-6
trityl tetrafluoroborate
| Conditions | Yield |
|---|---|
|
With
tetrafluoroboric acid diethyletherate;
In
propionic acid anhydride;
at 15 - 25 ℃;
for 1h;
Inert atmosphere;
|
71%
|
|
With
tetrafluoroboric acid;
In
diethyl ether; dichloromethane;
at 0 ℃;
|
42%
|
|
With
tetrafluoroboric acid; hydrogen;
In
diethyl ether; water;
at -60 ℃;
under 750.075 Torr;
Molecular sieve;
|
-
-
14104-20-2
silver tetrafluoroborate
-
-
76-83-5
trityl chloride
-
-
341-02-6
trityl tetrafluoroborate
| Conditions | Yield |
|---|---|
|
In
dichloromethane;
at 20 ℃;
|
69%
|
341-02-6 Upstream products
-
427-36-1
trityl fluoride
-
75-01-4
chloroethylene
-
76-83-5
trityl chloride
-
557-99-3
acetyl fluoride
341-02-6 Downstream products
-
51208-34-5
1,1-dimethoxy-2,6-diphenyl-4-trityl-1λ5 -phosphinine
-
55686-04-9
2-Phenyl-4-(triphenylmethyl)-2-oxazolin-5-on
-
6639-43-6
2,2,2-triphenylacetonitrile
-
51905-36-3
C29 H30
Relative Products
- 1,5-Diacetoxypentane
- 3-Methylhexane
- 4-(dimethoxymethyl)-1-(4-methylpentyl)cyclohexene
- 1-[[2-(diethylamino)ethyl]amino]-9H-thioxanthen-9-one
- QUINOLINE HYDROCHLORIDE
- 2-METHYL-4-UNDECANONE
- 2-ETHYLSUCCINIC ACID
- (R)-N-(2,4-dihydroxy-3,3-dimethylbutyryl)-beta-alanine, magnesium salt
- 4-hydroxy-5-[[(p-tolyl)sulphonyl]amino]naphthalene-2,7-disulphonic acid, sodium salt
- 4-METHOXYBENZENETHIOL
- 1-Nitroso-2-naphthol
- N-TERT-BUTYLISOPROPYLAMINE
- 2,3,5,6-TETRAMETHYL PHENOL
- 2-[2-(tetrahydro-2-furyl)ethyl]pyridine
- octahydro-3,5,5,8,8-pentamethylnaphthalene-2(1H)-one
- (E)-alpha-ethylidenepiperidine-1-acetaldehyde
- 3-[(2-aminocyclohexyl)methyl]-4-methylcyclohexylamine
- 1-(2-ethoxypropoxy)propan-2-ol
- Nonaethylene glycol
- 1-Octadecylpyridinium chloride