1842-26-8 Usage
Description
Silane, (2-fluorophenyl)trimethylis a colorless liquid with a molecular formula of C9H12F2Si. It belongs to the organosilicon compound family and is commonly used as a reagent in organic synthesis and as a surface modifier in various industries. This chemical is highly flammable and may react violently with water, air, or oxidizing agents. It should be handled with extreme caution and stored in a cool, dry, and well-ventilated area.
Uses
Used in Organic Synthesis:
Silane, (2-fluorophenyl)trimethylis used as a reagent in organic synthesis for its ability to modify and improve the properties of various organic compounds.
Used in Surface Modification:
Silane, (2-fluorophenyl)trimethylis used as a surface modifier to enhance the properties of materials in different industries, such as improving adhesion, durability, and resistance to environmental factors.
Used in Adhesives Industry:
Silane, (2-fluorophenyl)trimethylis used as a component in the manufacturing of adhesives for its ability to improve the bonding strength and durability of the adhesive products.
Used in Coatings Industry:
Silane, (2-fluorophenyl)trimethylis used as a component in the manufacturing of coatings to enhance the properties of the coatings, such as resistance to wear, corrosion, and environmental factors.
Used in Sealants Industry:
Silane, (2-fluorophenyl)trimethylis used as a component in the manufacturing of sealants to improve their sealing properties and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 1842-26-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1842-26:
(6*1)+(5*8)+(4*4)+(3*2)+(2*2)+(1*6)=78
78 % 10 = 8
So 1842-26-8 is a valid CAS Registry Number.
1842-26-8Relevant articles and documents
Synthesis of Distorted 1,8,13-Trisilyl-9-hydroxytriptycenes by Triple Cycloaddition of Ynolates to 3-Silylbenzynes
Yoshinaga, Tatsuro,Fujiwara, Takumi,Iwata, Takayuki,Shindo, Mitsuru
, p. 13855 - 13859 (2019)
1,8,13-Trialkyl(aryl)silyl-9-hydroxytriptycenes (trisilyltriptycenes) were synthesized by the triple addition of ynolates and 3-silylbenzynes with high regioselectivity. Benzene rings in the resulting triptycenes were highly distorted where the dihedral a
Cationic Chiral Fluorinated Oxazaborolidines. More Potent, Second-Generation Catalysts for Highly Enantioselective Cycloaddition Reactions
Mahender Reddy, Karla,Bhimireddy, Eswar,Thirupathi, Barla,Breitler, Simon,Yu, Shunming,Corey
, p. 2443 - 2453 (2016/03/08)
The coordination of chiral ligands to Lewis acid metal derivatives, a useful strategy for enantioselective, electrophilic catalysis, generally leads to a lower level of catalytic activity than that of the original uncomplexed compound. Activation by furth
Remote trimethylsilyl groups interfering with the ortho deprotonation of fluoroarenes and chloroarenes
Heiss, Christophe,Marzi, Elena,Mongin, Florence,Schlosser, Manfred
, p. 669 - 675 (2007/10/03)
(2-Fluorophenyl)trimethylsilane (2-F) and (2-chlorophenyl)-trimethylsilane (2-Cl) react with sec-butyllithium or lithium 2,2,6,6-tetramethylpiperidide under permutational hydrogen/metal interconversion (metalation) more slowly than, respectively, the corr
