21929-66-8

21929-66-8 structure
21929-66-8 structure

Name 3-(1-benzylimidazol-4-yl)-2-(phenylmethoxycarbonylamino)propanoic acid
Synonyms 2-(phenylmethoxycarbonylamino)-3-[1-(phenylmethyl)-4-imidazolyl]propanoic acid
1-Benzyl-N-[(benzyloxy)carbonyl]-L-histidine
N-Cbz-im-benzyl-L-histidine
1-Benzyl-N-[(benzyloxy)carbonyl]histidine
L-Histidine, N-[(phenylmethoxy)carbonyl]-1-(phenylmethyl)-
N-carbobenzyloxy-1-benzylhistidine
N-(carbobenzyloxy)-im-benzylhistidine
Description Z-His(Bzl)-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
Boiling Point 649.3±55.0 °C at 760 mmHg
Molecular Formula C21H21N3O4
Molecular Weight 379.409
Flash Point 346.5±31.5 °C
Exact Mass 379.153198
PSA 93.45000
LogP 2.82
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.613
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933290090

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21929-66-8 structure

21929-66-8

Literature: Journal of the Chemical Society, , p. 232,233 Helvetica Chimica Acta, , vol. 39, p. 229,243
Precursor  2

DownStream  0

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%