N-Boc-D-treonina, 95 %, Thermo Scientific Chemicals
N-Boc-D-treonina, 95 %, Thermo Scientific Chemicals
N-Boc-D-treonina, 95 %, Thermo Scientific Chemicals
N-Boc-D-treonina, 95 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

N-Boc-D-treonina, 95 %, Thermo Scientific Chemicals

CAS: 55674-67-4 | C9H17NO5 | 219.24 g/mol
Have Questions?
Cambiar vistabuttonViewtableView
Cantidad:
5 g
25 g
Número de catálogo H63647.14
también denominado H63647-14
Precio (USD)
-
Cantidad:
25 g
Pedido a granel o personalizado
Identificadores químicos
CAS55674-67-4
IUPAC Name(2R,3S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxybutanoic acid
Molecular FormulaC9H17NO5
InChI KeyLLHOYOCAAURYRL-NTSWFWBYSA-N
SMILESC[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C(O)=O
Ver más
EspecificacionesSpecification SheetHoja de especificaciones
Assay (HPLC)>94.0%
It is known to inhibit growth and cell wall synthesis of Mycobacterium smegmatis. Also used as a synthetic intermediate for the production of chiral antibiotics.

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.

Aplicaciones
Se sabe que inhibe el crecimiento y la síntesis de la pared celular de Mycobacterium smegmatis. También se utiliza como intermediario sintético para la producción de antibióticos quirales.

Solubilidad
Ligeramente soluble en agua.

Notas
Almacenar en un sitio fresco. Mantenga el recipiente bien cerrado en un lugar seco y bien ventilado. Almacenar lejos de agentes oxidantes.
RUO – Research Use Only

General References:

  1. Kunihiko Yabu; and Shozo Takahashi. Inhibition of Growth and Cell Wall Synthesis of Mycobacterium smegmatis by D-Threonine. Microbiology and Immunology. 1978, 22(2), 103-107.
  2. V. F. Pozdnev; N. N. Podgornova; N. K. Zentsova; G. I. Aukone; U. O. Kalei. Preparation of tert-butoxycarbonyl derivatives of amino acids using di-tert-butyl pyrocarbonate. Chemistry of Natural Compounds. 1979, 15(4), 471-476.