(S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

Modify Date: 2024-01-10 19:31:30

(S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate structure	Common Name	(S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate
	CAS Number	769922-77-2	Molecular Weight	400.43000
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₂₃H₂₀N₄O₃	Melting Point	N/A
	MSDS	Chinese USA	Flash Point	N/A
	Symbol	GHS07	Signal Word	Warning

Use of (S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

Z-Phe-Bt is a phenylalanine derivative[1].

Name	N-Cbz-L-Phe-Bt

Description	Z-Phe-Bt is a phenylalanine derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
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):1793-994.

Molecular Formula	C₂₃H₂₀N₄O₃
Molecular Weight	400.43000
Exact Mass	400.15400
PSA	86.11000
LogP	4.00010

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
RIDADR	NONH for all modes of transport

Precursor 0
DownStream 7
CAS#:23828-14-0 H-Gly-Phe-Ser-OH CAS#:6372-14-1 (S)-Cbz-Phenyla... CAS#:13126-07-3 Z-Phe-Met-OH CAS#:13123-00-7 Z-Phe-Val-OH
CAS#:13122-91-3 Z-Phe-Phe-OH CAS#:7669-64-9 Z-Phe-Pro-OH CAS#:37700-64-4 Z-Phe-Gly-Gly-OH

Benzotriazole-mediated syntheses of depsipeptides and oligoesters.

J. Org. Chem. 76 , 4884-4893, (2011)

Reactions of O-Pg(α-hydroxyacyl)benzotriazoles with (a) unprotected α-hydroxycarboxylic acids, (b) amino acids, and (c) amines afforded, respectively, chirally pure (a) oligoesters, (b) depsidipeptide...

Efficient preparation of aminoxyacyl amides, aminoxy hybrid peptides, and alpha-aminoxy peptides.

J. Org. Chem. 74th ed.,, 8690-8694, (2009)

N-(Pg-alpha-aminoxy acids) 1a-g are converted to N-(Pg-alpha-aminoxyacyl)benzotriazoles 2a-g, which react under mild conditions with amines, alpha-amino acids/alpha-dipeptides, and alpha-aminoxy acids...

Abdelmajeid, A.; Tala, S. R.; Amine, M. S.; Katritzky, A. R.

Synthesis , 2995-3005, (2011)

(S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

Use of (S)-Benzyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate

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