3-Fluoro-DL-phenylalanine structure
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Common Name | 3-Fluoro-DL-phenylalanine | ||
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CAS Number | 456-88-2 | Molecular Weight | 183.180 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 305.0±32.0 °C at 760 mmHg | |
Molecular Formula | C9H10FNO2 | Melting Point | -240ºC(dec.) | |
MSDS | Chinese USA | Flash Point | 138.3±25.1 °C |
Use of 3-Fluoro-DL-phenylalanineH-DL-Phe(3-F)-OH is a phenylalanine derivative[1]. |
Name | m-Fluoro-DL-phenylalanine |
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Synonym | More Synonyms |
Description | H-DL-Phe(3-F)-OH is a phenylalanine derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 305.0±32.0 °C at 760 mmHg |
Melting Point | -240ºC(dec.) |
Molecular Formula | C9H10FNO2 |
Molecular Weight | 183.180 |
Flash Point | 138.3±25.1 °C |
Exact Mass | 183.069550 |
PSA | 63.32000 |
LogP | 1.16 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.555 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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Hazard Codes | Xi: Irritant; |
Risk Phrases | R37 |
Safety Phrases | 24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2922499990 |
Precursor 5 | |
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DownStream 5 | |
HS Code | 2922499990 |
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Summary | HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0% |
Hidden overflow pathway to L-phenylalanine in Pseudomonas aeruginosa.
J. Bacteriol. 154(2) , 623-31, (1983) Pseudomonas aeruginosa is representative of a large group of pseudomonad bacteria that possess coexisting alternative pathways to L-phenylalanine (as well as to L-tyrosine). These multiple flow routes... |
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19F n.m.r. studies of conformational changes accompanying cyclic AMP binding to 3-fluorophenylalanine-containing cyclic AMP receptor protein from Escherichia coli.
Biochem. J. 287 ( Pt 2) , 627-32, (1992) A fluorine-containing analogue of the cyclic AMP (cAMP) receptor protein (CRP) from Escherichia coli was prepared by biosynthetic incorporation of 3-fluorophenylalanine (3-F-Phe). 19F n.m.r. studies o... |
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Fluorine-19 nuclear magnetic resonance spectroscopic study of fluorophenylalanine- and fluorotryptophan-labeled avian egg white lysozymes.
Biochemistry 33(17) , 5238-45, (1994) We report the 470-MHz (11.7 T) 19F solution nuclear magnetic resonance (NMR) spectra of 2-, 3-, and 4-fluorophenylalanine incorporated into the egg white lysozymes (EC 3.2.1.17) of chicken, pheasant, ... |
3-FLUORO-DL-PHENYLALANINE |
EINECS 207-272-1 |
DL-2-Amino-3-(3-fluorophenyl)propionic acid |
2-Amino-3-(3-fluorophenyl)propionic Acid |
2-Amino-3-(3-fluorophenyl)propanoic acid |
QVYZ1R CF &&DL Form |
DL-(3-Fluorophenyl)alanine |
m-Fluoro-DL-phenylalanine |
m-Fluorophenylalanine |
MFCD00004273 |
Phenylalanine, 3-fluoro- |
3-Fluorophenylalanine |
H-DL-Phe(3-F)-OH |