60764-82-1 Usage
Description
Triethylsilylmethanol, with the chemical formula (C2H5)3SiOH, is a colorless liquid characterized by a faint odor. It is a stable, non-reactive compound that serves as a versatile reagent in organic synthesis. Its properties include acting as a protective group for alcohols and phenols, a nucleophile in various organic reactions, and a silylating agent for alcohols and other functional groups. Triethylsilylmethanol is also noted for its relative safety in handling, exhibiting low toxicity and low flammability.
Uses
Used in Organic Synthesis:
Triethylsilylmethanol is used as a reagent for its ability to protect alcohols and phenols during organic chemistry reactions, ensuring the integrity of these functional groups until they are needed for subsequent reactions.
Used in Protective Group Chemistry:
In the field of protective group chemistry, Triethylsilylmethanol is used as a protective group to temporarily mask the reactivity of alcohols and phenols, allowing for selective reactions to occur at other sites on a molecule.
Used as a Nucleophile:
Triethylsilylmethanol is utilized as a nucleophile in various organic reactions, taking part in substitution and addition reactions where its electron-rich nature facilitates the formation of new chemical bonds.
Used as a Silylating Agent:
In the role of a silylating agent, Triethylsilylmethanol is used to transfer the trimethylsilyl group to other molecules, such as alcohols, thereby modifying their reactivity or solubility in organic solvents.
Used in the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its applications in organic synthesis and protective group chemistry, Triethylsilylmethanol can be inferred to have uses in the pharmaceutical industry for the synthesis of complex organic molecules, including potential drug candidates.
Used in the Chemical Research Industry:
In chemical research, Triethylsilylmethanol is used for its versatility in facilitating a range of reactions, enabling the exploration of new chemical pathways and the development of novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 60764-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60764-82:
(7*6)+(6*0)+(5*7)+(4*6)+(3*4)+(2*8)+(1*2)=131
131 % 10 = 1
So 60764-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H18OSi/c1-4-9(5-2,6-3)7-8/h8H,4-7H2,1-3H3
