Boc-D-Phg-OH structure
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Common Name | Boc-D-Phg-OH | ||
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CAS Number | 33125-05-2 | Molecular Weight | 251.278 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 382.6±25.0 °C at 760 mmHg | |
Molecular Formula | C13H17NO4 | Melting Point | 88-91 °C | |
MSDS | Chinese USA | Flash Point | 185.2±23.2 °C |
Use of Boc-D-Phg-OH(αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]benzeneacetic acid is a Glycine (HY-Y0966) derivative[1]. |
Name | (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-phenylacetic acid |
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Synonym | More Synonyms |
Description | (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]benzeneacetic acid is a Glycine (HY-Y0966) 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 | 1.2±0.1 g/cm3 |
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Boiling Point | 382.6±25.0 °C at 760 mmHg |
Melting Point | 88-91 °C |
Molecular Formula | C13H17NO4 |
Molecular Weight | 251.278 |
Flash Point | 185.2±23.2 °C |
Exact Mass | 251.115753 |
PSA | 66.84000 |
LogP | 2.95 |
Vapour Pressure | 0.0±0.9 mmHg at 25°C |
Index of Refraction | 1.557 |
Precursor 8 | |
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DownStream 7 | |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Boc-L-α-phenylglycine |
Boc-L-a-phenylglycine |
N-(tert-Butoxycarbonyl)-D-2-phenylglycine |
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-N-phenylglycine |
N-Boc-L-2-phenylglycine |
N-Boc-(S)-2-phenylglycine |
BOC-L-alpha-phenylglycine |
Boc-D-Phg-OH |
N-tert-butoxycarbonyl-L-phenylglycine |
[(tert-Butoxycarbonyl)amino](phenyl)acetic acid |
(S)-N-Boc-phenylglycine |
N-(tert-Butoxycarbonyl)-N-phenylglycine |
MFCD00065588 |
BOC-DL-(PHENYL)GLY-OH |
BOC-D-alpha-phenylglycine |
(S)-N-(tert-butoxycarbonyl)-2-phenylglycine |
Boc-L-phenylglycine |
(R)-2-((tert-Butoxycarbonyl)amino)-2-phenylacetic acid |
Benzeneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]- |
Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-phenyl- |
(S)-2-((tert-Butoxycarbonyl)amino)-2-phenylacetic acid |
N-Boc-D-Phenylglycine |
({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)(phenyl)acetic acid |
Boc-L-Phg-OH |
N-Boc-L-phenylglycine |
N-Boc-L-alpha-phenylglycine |
(2S)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid |
Boc-D-phenylglycine |
Boc-D-α-phenylglycine |
D-N-Boc-phenylglycine |
(S)-tert-Butoxycarbonylamino-phenyl-acetic acid |
Boc-Phg-OH |
N-(tert-Butoxycarbonyl)-L-2-phenylglycine |
N-Boc-D-2-phenylglycine |