86462-76-2 Usage
Uses
Used in Silicone Production:
((2R,3R)-3-[2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-ETHYL]-OXIRANYL)-METHANOL is used as a reactive agent for the production of silicones. Its epoxy and hydroxyl groups enable it to act as a crosslinker, providing strength and flexibility to the resulting polymers.
Used in Resin Production:
((2R,3R)-3-[2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-ETHYL]-OXIRANYL)-METHANOL is used as a reactive agent in the production of resins. Its chemical structure allows it to form strong bonds with other components, resulting in high-performance resins with improved properties.
Used in Polymeric Materials:
((2R,3R)-3-[2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-ETHYL]-OXIRANYL)-METHANOL is used as a building block in the production of various polymeric materials. Its unique properties, such as strength, flexibility, and stability, make it an important component in the development of advanced materials for various industries.
Used in Pharmaceutical Industry:
((2R,3R)-3-[2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-ETHYL]-OXIRANYL)-METHANOL is used as a protective group in the synthesis of pharmaceutical compounds. The tert-butyl-dimethyl-silanyloxy group provides stability and protection during the synthesis process, preventing premature reactions with other chemicals.
Used in Coatings Industry:
((2R,3R)-3-[2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-ETHYL]-OXIRANYL)-METHANOL is used as a crosslinking agent in the production of coatings. Its ability to form strong bonds with other components results in coatings with improved durability and performance.
Used in Adhesives Industry:
((2R,3R)-3-[2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-ETHYL]-OXIRANYL)-METHANOL is used as a reactive component in the formulation of adhesives. Its epoxy and hydroxyl groups enable it to form strong bonds with various substrates, resulting in adhesives with high bonding strength and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 86462-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86462-76:
(7*8)+(6*6)+(5*4)+(4*6)+(3*2)+(2*7)+(1*6)=162
162 % 10 = 2
So 86462-76-2 is a valid CAS Registry Number.
86462-76-2Relevant academic research and scientific papers
Total synthesis of (-)-dactylynes
Gao, Lian-Xun,Murai, Akio
, p. 745 - 774 (2007/10/03)
The first total synthesis of (-)-dactylyne (1) and (-)-isodactylyne (2), which have been isolated from sea hare, is described in detail. Critical steps in the synthesis include a stereoselective construction as well as an intramolecular ring closure of 32, and the effective double elongation reactions (59 → 63 and 64, 67 → 68, and 70 → 71).
Enantioselective Routes toward 1β-Methylcarbapenems from Chiral Aziridines
Tanner, David,He, Hua Ming
, p. 6079 - 6086 (2007/10/02)
This paper describes two enantioselective aziridine-based routes toward 1β-methylthienamycin, 2, and related carbapenems, the key steps being completely regioselective ring-opening reactions of the chiral aziridines 7 and 10 with AlMe3. - Key Words: 1β-me
The first enantiocontrolled synthesis of (3S,8S)-(-)-4,6-decadiyne-1,3,8-triol isolated from a toxic mushroom Gymnopilus spectabilis
Takano,Sugihara,Ogasawara
, p. 2797 - 2798 (2007/10/02)
The first synthesis of (3S,8S)-(-)-4,6-decadiyne-1,3,8-triol, isolated from a toxic mushroom Gymnopilus spectabilis, has been achieved by employing the chiral 3-hydroxyalkyne formation reaction as the key step.
