17903-57-0 Usage
Uses
Used in Organic Synthesis:
(4-(trimethylsilyl)phenyl)methanol is used as a reagent for the protection of hydroxyl groups in organic molecules. This application is crucial in organic synthesis to prevent unwanted reactions from occurring at the hydroxyl group, allowing chemists to selectively modify other parts of the molecule.
Used in Pharmaceutical Production:
(4-(trimethylsilyl)phenyl)methanol is utilized in the production of pharmaceuticals, where its ability to protect hydroxyl groups can be advantageous in the synthesis of complex drug molecules. Its use in this industry helps facilitate the creation of new and effective medications.
Used in Agrochemical Production:
(4-(trimethylsilyl)phenyl)methanol is also employed in the production of agrochemicals, which includes pesticides, herbicides, and other chemicals used in agriculture. Its role in this industry is similar to its use in pharmaceuticals, providing a means to protect hydroxyl groups during the synthesis of various agrochemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 17903-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17903-57:
(7*1)+(6*7)+(5*9)+(4*0)+(3*3)+(2*5)+(1*7)=120
120 % 10 = 0
So 17903-57-0 is a valid CAS Registry Number.
17903-57-0Relevant academic research and scientific papers
A mild method for regioselective labeling of aromatics with radioactive iodine
Ronnest, Mads H.,Nissen, Felix,Pedersen, Palle J.,Larsen, Thomas O.,Mier, Walter,Clausen, Mads H.
supporting information, p. 3970 - 3973 (2013/07/19)
A novel technique to label ortho-, meta-, and para-trimethylsilyl- substituted aryl substituents with radioactive iodide is described. The method takes advantage of the ipso-directing and activating properties of trimethylsilyl substituents on the arenes.
DTBB-catalysed lithiation of chlorinated benzylic chlorides, alcohols, thiols or amines
Gomez, Cecilia,Huerta, Fernando F.,Yus, Miguel
, p. 1853 - 1866 (2007/10/03)
The reaction of chlorinated benzyl chlorides (I) with an excess of lithium powder and a catalytic amount of DTBB (4 mol %) in the presence of different electrophiles [Pr(i)CHO, Bu(t)CHO, Et2CO, (CH2)5CO, PhCOMe, Me3/
