BOC-D-PHG-OH

Modify Date: 2024-01-02 08:00:05

BOC-D-PHG-OH Structure
BOC-D-PHG-OH structure
Common Name BOC-D-PHG-OH
CAS Number 2900-27-8 Molecular Weight 251.278
Density 1.2±0.1 g/cm3 Boiling Point 407.2±38.0 °C at 760 mmHg
Molecular Formula C13H17NO4 Melting Point 88-91ºC
MSDS USA Flash Point 200.1±26.8 °C

 Use of BOC-D-PHG-OH


Boc-Phg-OH is a Glycine (HY-Y0966) derivative[1].

 Names

Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-phenylacetic acid
Synonym More Synonyms

 BOC-D-PHG-OH Biological Activity

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.

 Chemical & Physical Properties

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.

 Safety Information

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

 Synthetic Route

 Customs

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%

 Synonyms

Boc-L-α-phenylglycine
Boc-L-a-phenylglycine
(S)-N-(tert-butoxycarbonyl)-2-phenylglycine
Boc-L-phenylglycine
Benzeneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-
N-Boc-L-2-phenylglycine
N-Boc-(S)-2-phenylglycine
MFCD00062043
(S)-2-((tert-Butoxycarbonyl)amino)-2-phenylacetic acid
({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)(phenyl)acetic acid
(2S)-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)(phenyl)acetic acid
Boc-L-Phg-OH
BOC-L-alpha-phenylglycine
(2S)-[(tert-Butoxycarbonyl)amino](phenyl)acetic acid
N-Boc-L-alpha-phenylglycine
N-tert-butoxycarbonyl-L-phenylglycine
[(tert-Butoxycarbonyl)amino](phenyl)acetic acid
(2S)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid
(S)-N-Boc-phenylglycine
Benzeneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)-
(S)-tert-Butoxycarbonylamino-phenyl-acetic acid
Boc-Phg-OH
N-(tert-Butoxycarbonyl)-L-2-phenylglycine
BOC-DL-(PHENYL)GLY-OH
BOC-D-PHG-OH
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