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132388-68-2

132388-68-2 structure
132388-68-2 structure

Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-(tritylamino)butanoic acid
Synonyms N-ALPHA-T-BOC-BETA-TRITYL-L-ASPAGINE
N-ALPHA-T-BUTOXYCBONYL-N-BETA-TRITYL-L-ASPAGINE
Nα-(tert-Butoxycbonyl)-Nγ-trityl-L-aspagine
N-(tert-Butoxycarbonyl)-N-trityl-L-asparagine
BOC-ASN(TRT)-OH
N-tert-Butoxycbonyl-β-trityl-L-aspagine
Nα-tert-Butoxycbonyl-Nγ-trityl-L-aspagine
N-Alpha-t-Boc-N-beta-trityl-asparagine
N-BETA-TERT-BUTOXYCBONYL-N-GAMMA-TRITYL-L-ASPAGINE
Boc-N-beta-Trityl-L-aspaD23-RAgine
N-ALPHA-T-BOC-N-BETA-TRITYL-ASPAGINE
L-Aspagine,N2-[(1,1-dimethylethoxy)carbonyl]-N-(triphenylmethyl)
BOC-N-GAMMA-TRITYL-L-ASPAGINE
N2-(tert-Butoxycbonyl)-N4-trityl-L-aspagine
(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-4-oxo-4-(tritylamino)butanoic acid
Nalpha-Boc-Ngamma-trityl-L-aspagine Boc-Asn(Trt)-OH
(Tert-Butoxy)carbonyl Asn(Trt)-OH
Boc-N-triphenylmethyl-L-aspagine
n(alpha)-boc-n(gamma)-trityl-l-aspa-gine
BOC-L-ASPAGINE(TRITYL)
Nalpha-tert-Butoxycarbonyl-Ngamma-trityl-L-asparagine
Nalpha-t-Butoxycbonyl-Ng-trityl-L-aspagine
Boc-Asn(Trt)-OH N-α-Boc-N-γ-trityl-L-aspagine
Nalpha-Boc-Ngamma-trityl-L-asparagine
(S)-2-((tert-Butoxycarbonyl)amino)-4-oxo-4-(tritylamino)butanoic acid
Nα-Boc-Nγ-trityl-L-asparagine
Nα-Boc-Nγ-trityl-L-aspagine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-N-trityl-L-asparagine
Tert butoxycbonyl-N beta triphenylmethyl L-aspagine
BOC-L-(TRITYL)ASPAGINE
Nα-tert-Butoxycbonyl-Nγ-trityl-L-aspagine >
Nα-Boc-Nγ-trityl-L-aspagine (HPLC, Chiral purity)
(S)-2-((tert-Butoxycbonyl)amino)-4-oxo-4-(tritylaMino)butanoic acid
Boc-N-beta-Trityl-L-asparagine
Boc-N-beta-Trityl-L-aspagine //BP
Boc-N-beta-Trityl-L
N-ALPHA-BOC-N-GAMMA-TRITYL-L-APAGINE
Boc-N-β-trityl-L-aspagine
(2S)-2-[(2-methylpropan-2-yl)oxycbonylamino]-4-oxo-4-(tritylamino)butanoicaci
N-α-Boc-N-γ-trityl-L-aspagine
N-a-t-Boc-N-g-trityl-L-aspagine
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-4-oxo-4-(tritylamino)butanoic acid
(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-[(triphenylmethyl)cbamoyl]propanoic acid
N-Boc-N'-trityl-L-asparagine
Nα-tert-Butoxycarbonyl-Nγ-trityl-L-asparagine
N^a-Boc-N^y-trityl-L-aspagine
N-α-t-Boc-N-γ-trityl-aspagine
(2S)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-4-oxo-4-[(triphenylmethyl)amino]butanoic acid
NALPHA-TERT-BUTOXYCBONYL-NGAMMA-TRITYL-L-ASPAGINE
BOC-N-BETA-TRITYL-L-ASPAGINE
Description N2-(tert-Butoxycarbonyl)-N4-trityl-L-asparagine is an aspartic acid 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 711.0±60.0 °C at 760 mmHg
Melting Point 205ºC
Molecular Formula C28H30N2O5
Molecular Weight 474.548
Flash Point 383.8±32.9 °C
Exact Mass 474.215485
PSA 104.73000
LogP 5.88
Vapour Pressure 0.0±2.4 mmHg at 25°C
Index of Refraction 1.582
Storage condition Store at 0°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases 22-24/25
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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