CAS 135065-71-3: (R)-N-Boc-2-Hydroxymethylmorpholine
Formula:C10H19NO4
InChI:InChI=1/C10H19NO4/c1-10(2,3)15-9(13)11-4-5-14-8(6-11)7-12/h8,12H,4-7H2,1-3H3/t8-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCO[C@H](C1)CO
Synonyms:- (R)-2-Hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester
- 2-(Hydroxymethyl)morpholine-4-carboxylic acid (R)-tert-butyl ester
- (R)-4-Boc-2-Hydroxymethyl-Morpholine
- tert-butyl (2R)-2-(hydroxymethyl)morpholine-4-carboxylate
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Found 5 products.
(R)-N-Boc-2-hydroxymethylmorpholine, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C10H19NO4Purity:99%Molecular weight:217.27(R)-4-Boc-2-hydroxymethyl-morpholine
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:217.26499938964844tert-Butyl (2R)-2-(hydroxymethyl)morpholine-4-carboxylate
CAS:tert-Butyl (2R)-2-(hydroxymethyl)morpholine-4-carboxylatePurity:98+%Molecular weight:217.26g/mol(R)-N-Boc-2-Hydroxymethylmorpholine
CAS:(R)-N-Boc-2-Hydroxymethylmorpholine is an enantioselective synthesis of a drug. It is used in the reductive amination of aldehydes with ammonia, which has been shown to be operationally enantioselective. (R)-N-Boc-2-Hydroxymethylmorpholine undergoes an intramolecular reaction that results in the formation of an azido group. This asymmetric reaction is catalyzed by palladium, and the product can be used for the reductive amination of aldehydes with ammonia.Formula:C10H19NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:217.26 g/mol(R)-N-Boc-2-Hydroxymethylmorpholine
CAS:Formula:C10H19NO4Purity:98%Color and Shape:SolidMolecular weight:217.2622
