(S)-Cbz-Phenylalaninol

Modify Date: 2024-01-02 22:09:19

(S)-Cbz-Phenylalaninol structure	Common Name	(S)-Cbz-Phenylalaninol
	CAS Number	6372-14-1	Molecular Weight	285.338
	Density	1.2±0.1 g/cm3	Boiling Point	489.0±45.0 °C at 760 mmHg
	Molecular Formula	C₁₇H₁₉NO₃	Melting Point	90-94ºC
	MSDS	Chinese USA	Flash Point	249.6±28.7 °C

Use of (S)-Cbz-Phenylalaninol

Z-Phenylalaninol is an alanine derivative[1].

Name	(S)-Cbz-Phenylalaninol
Synonym	More Synonyms

Description	Z-Phenylalaninol is an alanine 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):1793-1110.

Density	1.2±0.1 g/cm3
Boiling Point	489.0±45.0 °C at 760 mmHg
Melting Point	90-94ºC
Molecular Formula	C₁₇H₁₉NO₃
Molecular Weight	285.338
Flash Point	249.6±28.7 °C
Exact Mass	285.136505
PSA	58.56000
LogP	3.25
Vapour Pressure	0.0±1.3 mmHg at 25°C
Index of Refraction	1.583
Storage condition	2~8°C

(S)-Cbz-Phenylalaninol MSDS(Chinese)

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	T+
Safety Phrases	S22-S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2924299090

Precursor 8
CAS#:1161-13-3 N-Cbz-L-Phenyla... CAS#:13139-17-8 N-(Benzyloxycar... CAS#:3182-95-4 H-Phe-ol CAS#:501-53-1 Benzyl chloroformate
CAS#:35909-92-3 Z-Phe-OMe CAS#:28709-70-8 N-CARBOBENZYLOX... CAS#:55740-07-3 (4S)-4-benzyl-5... CAS#:59830-60-3 (S)-(-)-2-(Benz...
DownStream 8
CAS#:3182-95-4 H-Phe-ol CAS#:1161-13-3 N-Cbz-L-Phenyla... CAS#:2448-45-5 Z-D-Phe-OH CAS#:856570-20-2 (S)-2-BENZYL-3-...
CAS#:59830-60-3 (S)-(-)-2-(Benz... CAS#:63-91-2 L-Phenylalanine CAS#:13122-99-1 Cbz-Phe-Gly-OH CAS#:37700-64-4 Z-Phe-Gly-Gly-OH

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%

Preparation of Aminoalkyl Chlorohydrin Hydrochlorides: Key Building Blocks for Hydroxyethylamine-Based HIV Protease Inhibitors.

J. Org. Chem. 61 , 3635, (1996)

Enantiomerically pure N,N-dibenzyl-alpha-amino aldehydes reacted with (chloromethyl)lithium, generated in situ from bromochloromethane and lithium metal, to give predominantly erythro aminoalkyl epoxi...

Stereoselective Synthesis of HIV-1 Protease Inhibitor, DMP 323.

J. Org. Chem. 61 , 444, (1996)

DMP 323, a potent HIV-1 protease inhibitor, has been synthesized by an efficient stereoselective process, amenable to large scale preparations. The core C(2) symmetric diol was synthesized by a stereo...

Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas.

J. Med. Chem. 39 , 3514, (1996)

High-resolution X-ray structures of the complexes of HIV-1 protease (HIV-1PR) with peptidomimetic inhibitors reveal the presence of a structural water molecule which is hydrogen bonded to both the mob...

Benzyl [(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamate

Carbamic acid, N-[(1S)-2-hydroxy-1-(phenylmethyl)ethyl]-, phenylmethyl ester

benzyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamate

Benzyl [(2S)-1-hydroxy-3-phenyl-2-propanyl]carbamate

Benzyl (1-hydroxy-3-phenylpropan-2-yl)carbamate

Z-L-phenylalaninol;; (S)-2-(Z-amino)-3-phenyl-1-propanol

MFCD00191138

Z-Phenylalaninol

Z-Phe-ol