Z-D-ALA-NH2
- Product Name
- Z-D-ALA-NH2
- CAS No.
- 151378-81-3
- Chemical Name
- Z-D-ALA-NH2
- Synonyms
- Z-D-ALA-NH2;CBZ-D-Ala-NH2;Z-D-ALANINE-NH2;CBZ-D-ALANINAMIDE;Z-D-ALANINE AMIDE;N-Cbz-D-alanine amide;(R)-2-(Cbz-amino)propanamide;Z-D-alanine amide≥ 98% (HPLC);N-Benzyloxycarbonyl-D-alaninamide;N-ALPHA-CARBOBENZOXY-D-ALANINE AMIDE
- CBNumber
- CB7155851
- Molecular Formula
- C11H14N2O3
- Formula Weight
- 222.24
- MOL File
- 151378-81-3.mol
Z-D-ALA-NH2 Property
- Melting point:
- 132-134 °C
- Boiling point:
- 443.8±38.0 °C(Predicted)
- Density
- 1.199±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 11.17±0.46(Predicted)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- A614010
- Product name
- Z-D-Ala-NH2
- Packaging
- 250mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- 260725
- Product name
- Z-D-alanine amide
- Packaging
- 1g
- Price
- $333
- Updated
- 2021/12/16
- Product number
- FA48887
- Product name
- Z-D-alanine amide
- Packaging
- 5G
- Price
- $251.1
- Updated
- 2021/12/16
- Product number
- FA48887
- Product name
- Z-D-alanine amide
- Packaging
- 2g
- Price
- $97.1
- Updated
- 2021/12/16
- Product number
- 7872AH
- Product name
- Z-D-Ala-NH2
- Packaging
- 25g
- Price
- $107
- Updated
- 2021/12/16
Z-D-ALA-NH2 Chemical Properties,Usage,Production
Chemical Properties
White to off-white powder
Synthesis
26607-51-2
151378-81-3
General procedure for the synthesis of benzyl (R)-(1-amino-1-oxo-2-propyl)carbamate from (R)-2-((benzyloxy)carbonyl)amino)propionic acid: to a colorless solution of 150 mg (0.50 mmol) of (R)-2-((benzyloxy)carbonyl)amino)propionic acid in 10 mL of tetrahydrofuran (THF) was added at 0 °C 67 μL ( 0.70 mmol, 1.4 eq.) ethyl chloroformate and 209 μL (1.5 mmol, 3.0 eq.) triethylamine. After stirring for 30 min at 0 °C, 0.75 mL of 1.0 M aqueous ammonium chloride (0.75 mmol, 1.5 equiv) was added to the colorless suspension at 0 °C. The mixture was continued to be stirred at 0 °C for 30 min, after which 5 mL of water was added to the reaction mixture. The colorless clear solution was extracted with 30 mL of ethyl acetate and the aqueous layer was extracted with another 20 mL of ethyl acetate. The organic layers were combined, washed with 5 mL of saturated brine and dried with anhydrous magnesium sulfate. The crude product was purified by silica gel column chromatography using ethyl acetate as eluent to give 129 mg (86% yield) of the target product (R)-(1-amino-1-oxo-2-propyl)carbamic acid benzyl ester.
References
[1] Tetrahedron Asymmetry, 2017, vol. 28, # 12, p. 1690 - 1699
[2] Bioorganic and Medicinal Chemistry Letters, 1996, vol. 6, # 6, p. 631 - 636
[3] Journal of Medicinal Chemistry, 2000, vol. 43, # 10, p. 1910 - 1926
[4] Chemistry Letters, 2013, vol. 42, # 6, p. 580 - 582
Z-D-ALA-NH2 Preparation Products And Raw materials
Raw materials
Preparation Products
Z-D-ALA-NH2 Suppliers
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