N-Boc-glycine methyl ester, 97%, Thermo Scientific Chemicals
N-Boc-glycine methyl ester, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

N-Boc-glycine methyl ester, 97%, Thermo Scientific Chemicals

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Quantity:
5 mL
25 mL
Catalog number H59234.AA
also known as H59234-AA
Price (EUR)/ Each
38,79
Online exclusive
43.10 
Save 4,31 (10%)
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Quantity:
5 mL
Request bulk or custom format
Price (EUR)/ Each
38,79
Online exclusive
43.10 
Save 4,31 (10%)
Add to cart
N-Boc-glycine methyl ester, 97%, Thermo Scientific Chemicals
Catalog numberH59234.AA
Price (EUR)/ Each
38,79
Online exclusive
43.10 
Save 4,31 (10%)
-
Add to cart
Chemical Identifiers
CAS31954-27-5
IUPAC Namemethyl 2-{[(tert-butoxy)carbonyl]amino}acetate
Molecular FormulaC8H15NO4
InChI KeyPHUZOEOLWIHIKH-UHFFFAOYSA-N
SMILESCOC(=O)CNC(=O)OC(C)(C)C
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)>96.0%
It is used as a pharmaceutical, chemical, paint and dye intermediate.

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.

Applications
It is used as a pharmaceutical, chemical, paint and dye intermediate.

Notes
Store at room temperature. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Ishiwata Hiroyuki.; Sone Hiroki.; Kigoshi Hideo.; Yamada Kiyoyuki. Enantioselective total synthesis of doliculide, a potent cytotoxic cyclodepsipeptide of marine origin and structure-cytotoxicity relationships of synthetic doliculide congeners. Tetrahedron. 1994, 50 (45),12853-12882.
  2. Andrew G. Myers.; James L. Gleason.; Taeyoung Yoon. Practical method for the synthesis of D- or L-.alpha.-amino acids by the alkylation of (+)- or (-)-pseudoephedrine glycinamide. J. Am. Chem. Soc. 1995, 117 (32),8488-8489.