1. Home
  2. Silane, (1,1-dimethylethyl)dimethyl[(2R)-oxiranylmethoxy]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Silane, (1,1-dimethylethyl)dimethyl[(2R)-oxiranylmethoxy]-

CC([Si](OC[C@@H]1OC1)(C)C)(C)C Request for Quotation
Chemical Name: Silane, (1,1-dimethylethyl)dimethyl[(2R)-oxiranylmethoxy]-
CAS Number: 124150-87-4
Product Number: AG000LLO(AGN-PC-0O0OTF)
Synonyms:
MDL No:
Molecular Formula: C9H20O2Si
Molecular Weight: 188.3394

Identification/Properties

Properties
BP:
195-199 °C/760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.4310

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H227-H302-H315-H319-H335
Precautionary Statements:
P210-P231+P232-P235-P261-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P309+P311-P370+P378-P403+P233-P403+P235
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(R)-tert-Butyldimethyl(oxiran-2-ylmethoxy)silane, also known as $name$, is a versatile compound that finds widespread application in chemical synthesis. This compound is particularly valued for its role as a chiral building block in organic reactions, facilitating the creation of enantiomerically pure products. In asymmetric synthesis, (R)-tert-Butyldimethyl(oxiran-2-ylmethoxy)silane serves as a valuable reagent for introducing chiral centers with high selectivity. Its unique structure enables the formation of complex molecules with defined stereochemistry, making it a crucial tool in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, this compound demonstrates excellent reactivity and compatibility with a variety of functional groups, further expanding its utility in the realm of chemical synthesis.