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2900-27-8

2900-27-8 structure
2900-27-8 structure

Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-phenylacetic acid
Synonyms BOC-D-A-PHENYLGLYCINE
N-Boc-(S)-2-phenylglycine
N-(tert-Butoxycbonyl)-L-2-phenylglycine >
(2S)-[(tert-butoxycbonyl)amino](phenyl)ethanoic acid
(S)-N-tert-butoxycbonyl-2-phenylgylcine
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-2-phenylacetic acid
N-ALPHA-T-BOC-D-PHENYLGLYCINE
N-tert-butoxycarbonyl-L-phenylglycine
NALPHA-tert-Butoxycbonyl-D-phenylglycine
Boc-Phg-OH Boc-L-Phenylglycine
T-BUTOXYCBONYL-D-PHENYLGLYCINE
N-(tert-Butoxycbonyl)-L-2-phenylglycine, (LC)
BOC-PHG-OH
(S)-N-(tert-butoxycarbonyl)-2-phenylglycine
Benzeneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)
BOC-D-PHG-OH //BP
(S)-Boc-2-aminophenylacetic acid
({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)(phenyl)acetic acid
(S)-2-(Boc-amino)-2-phenylacetic Acid
(2S)-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)(phenyl)acetic acid
Boc-L-Phg-OH
N-ALPHA-T-BUTYLOXYCBONYL-D-PHENYLGLYCINE
N-Boc-L-alpha-phenylglycine
(2S)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid
(R)-TERT-BUTOXYCBONYLAMINO-PHENYL-ACETIC ACID
(S)-tert-Butoxycarbonylamino-phenyl-acetic acid
Boc-Phg-OH
(Tert-Butoxy)carbonyl Phg-OH
N-Boc-L-2-phenylglycine,e.e
BOC-D-(PHENYL)GLY-OH
N-BOC-D-PHENYLGLYCINE
Boc-L-α-phenylglycine
Boc-L-a-phenylglycine
N-(tert-butoxycbonyl)-L-alpha-phenylglycine
N-Boc-L-2-phenylglycine Boc-Phg-OH
N-Boc-L-2-phenylglycine
MFCD00062043
BOC-L-alpha-phenylglycine
BOC-D-PHG
(S)-2-((tert-Butoxycbonyl)amino)-2-phenylacetic acid
(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-2-phenyla
[(tert-Butoxycarbonyl)amino](phenyl)acetic acid
(S)-N-Boc-phenylglycine
BOC-L-Phenylglycine extrapure
BOC-L-PHENYLGLYCINE(BOC-PHG-OH)
BOC-DL-(PHENYL)GLY-OH
(2S)-2-[(tert-butoxycbonyl)amino]-2-phenylethanoic acid
Boc-L-phenylglycine
RECHEM EM WB 0178
(S)-Boc-L-Phenylglycine
(S)-2-((tert-Butoxycarbonyl)amino)-2-phenylacetic acid
(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-2-phenylacetic acid
2-(tert-butoxycbonyl)-2-phenylacetic acid
BOC-D-ALPHA-PHENYLGLYCINE
N-(tert-Butoxycbonyl)-L-2-phenylglycine
(2S)-[(tert-Butoxycarbonyl)amino](phenyl)acetic acid
N-ALPHA-TERT-BUTYLOXYCBONYL-D-PHENYLGLYCINE
N-tert-Butoxycbonyl-L-phenylglycine
N-(tert-Butoxycarbonyl)-L-2-phenylglycine
(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-2-phenylaceticaci
Boc-Phg-OH~N-(tert-Butoxycbonyl)-L-phenylglycine
Description Boc-Phg-OH is a Glycine (HY-Y0966) derivative[1].
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

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Density 1.2±0.1 g/cm3
Boiling Point 407.2±38.0 °C at 760 mmHg
Melting Point 88-91ºC
Molecular Formula C13H17NO4
Molecular Weight 251.278
Flash Point 200.1±26.8 °C
Exact Mass 251.115753
PSA 75.63000
LogP 2.74
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.532
Storage condition Store at RT.
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090
HS Code 2924299090
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%
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