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35899-43-5

35899-43-5 structure
35899-43-5 structure

Name Boc-L-Histidine(Tosyl)
Synonyms N-alpha-BOC-N(im)-tosyl-L-histidine
1-[(4-Methylphenyl)sulfonyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-histidine
L-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-1-[(4-methylphenyl)sulfonyl]-
Boc-His(Tos)-OH
(2S)-3-[1-(4-methylphenyl)sulfonylimidazol-4-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Nalpha-(tert-Butoxycarbonyl)-tele-(p-toluenesulfonyl)-L-histidine
Nα-Boc-τ-tosyl-L-histidine
Boc-L-His(Tos)-OH
N-(tert-Butoxycarbonyl)-1-[(4-methylphenyl)sulfonyl]-L-histidine
(S)-2-((tert-Butoxycarbonyl)amino)-3-(1-tosyl-1H-imidazol-4-yl)propanoic acid
MFCD00065967
Nα-(tert-Butoxycarbonyl)-τ-(p-toluenesulfonyl)-L-histidine
Description Boc-His(Tos)-OH is a histidine 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 1.3±0.1 g/cm3
Melting Point ~125 °C (dec.)
Molecular Formula C18H23N3O6S
Molecular Weight 409.457
Exact Mass 409.130768
PSA 135.97000
LogP 2.14
Index of Refraction 1.595
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes T+
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933290090
HS Code 2933290090
Summary 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%