ChemicalBook > Product Catalog > Biochemical Engineering > Amino Acids and Derivatives > Glycine derivative > D-Allylglycine
D-Allylglycine
D-Allylglycine Basic information
- Product Name:
- D-Allylglycine
- Synonyms:
-
- 3-VINYL-D-ALANINE
- D-C-ALLYLGLYCINE
- D-ALLYLGLYCINE
- D-ALPHA-ALLYL-GLY
- D-ALPHA-ALLYL-GLYCINE
- D-2-AMINO-4-PENTENOIC ACID
- H-ALLYL-D-GLYCINE
- H-D-GLY(ALLYL)-OH
- CAS:
- 54594-06-8
- MF:
- C5H9NO2
- MW:
- 115.13
- Product Categories:
-
- Amino Acids 13C, 2H, 15N
- a-amino
- Amino Acids
- Amino Acid Derivatives
- Amino Acids & Derivatives
- unnatural amino acids
- Chiral Reagent
- API
- Mol File:
- 54594-06-8.mol
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D-Allylglycine Chemical Properties
- Melting point:
- 239.3-241.2 °C
- Boiling point:
- 231.0±33.0 °C(Predicted)
- alpha
- 37 º (c=2% in H2O)
- Density
- 1.098±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- Water (Slightly)
- form
- Solid
- pka
- 2.22±0.10(Predicted)
- color
- White to Light Beige
- BRN
- 1721511
- Stability:
- Light Sensitive
- InChIKey
- WNNNWFKQCKFSDK-SCSAIBSYSA-N
- CAS DataBase Reference
- 54594-06-8(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 22-24/25-36-26
- WGK Germany
- 3
- HS Code
- 29224999
MSDS
- Language:English Provider:SigmaAldrich
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D-Allylglycine Usage And Synthesis
Chemical Properties
Off-White Solid
Uses
D-Allylglycine is a new chiral glycine equivalent, it is used for the preparation of enantiomerically pure a-tertiary and a-quaternary a-amino acids. A Bacillus spore germination alanine analog.
Biochem/physiol Actions
D-allylglycine is the enantiomer of L-allylglycine, a glutamate decarboxylase (GAD) inhibitor used in GABA research. D-allylglycine may be used as a control supplement versus L-allylglycine in GABA research. D-allylglycine is used in the organic synthesis of cyclic opioid peptide agonists and antagonists.
D-AllylglycineSupplier
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- sales@pharmablock.com
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D-Allylglycine(54594-06-8)Related Product Information
- Allyl glycidyl ether
- Allyl bromide
- Glycine
- 6-Aminocaproic acid
- Allyl chloride
- Sodium allylsulfonate
- L-2-Allylglycine Hydrochloride
- (S)-ALPHA-METHYL-ALLYLGLYCINE
- DL-ALLYLGLYCINE
- DL-ALLYLGLYCINE,DL-C-ALLYLGLYCINE,rac-(R*)-2-Allylglycine,ALLYLGLYCINE[ALLYGLY],DL-Allylglycine 2-Amino-4-pentenoic acid
- (R)-2-Amino-2-methyl-4-pentenoic acid
- Allylamine
- BOC-D-ALLYLGLYCINE-DCHA,BOC-D-ALLYLGLYCINE DCHA SALT,BOC-D-ALLYLGLYCINE DICYCLOHEXYLAMINESALT,BOC-D-ALLYLGLYCINE DICYCLOHEXYLAMMONIUM SALT
- Boc-L-2-allylglycine dicyclohexylamine salt
- (S)-N-BOC-ALLYLGLYCINE,(S)-N-Boc-allylglycine(e.e.)
- (R)-N-boc-Allylglycine(e.e.),D-2-Allylglycine, N-BOC protected dicylohexylamine salt,Boc-D-Allylglycine,(R)-N-BOC-ALLYLGLYCINE
- D-C-ALLYLGLYCINE,D-2-ALLYLGLYCINE HYDROCHLORIDE
- N-ACETYL-DL-ALLYLGLYCINE