(S)-Cbz-Phenylalaninol

Suppliers

Names

[ Name ]:
(S)-Cbz-Phenylalaninol

[Synonym ]:
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

Chemical & Physical Properties

[ 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

MSDS

Click to get detail MSDS

Safety Information

[ 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 & DownStream

Precursor

N-Cbz-L-Phenylalanine
N-(Benzyloxycarbonyloxy)succinimide
H-Phe-ol
Benzyl chloroformate
Z-Phe-OMe
N-CARBOBENZYLOXY-D-PHENYLALANINE+
(4S)-4-benzyl-5-oxo-1,3-oxazolidine-3-carboxylic acid benzyl ester
(S)-(-)-2-(Benzylcarbonylamino)-3-phenylpropanal

DownStream

H-Phe-ol
N-Cbz-L-Phenylalanine
Z-D-Phe-OH
(S)-2-BENZYL-3-(BENZYLOXY)-3-OXOPROPANE-1-SULFONIC ACID
(S)-(-)-2-(Benzylcarbonylamino)-3-phenylpropanal
L-Phenylalanine
Cbz-Phe-Gly-OH
Z-Phe-Gly-Gly-OH

Customs

[ 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%

Articles

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...

(S)-Cbz-3-Amino-4,4,4-trifluorobutanoic acid
Cbz-phenylalaninol methanesulfonate
POLY-S-CBZ-L-CYSTEINE MOL WT 5000-15000
Pentanoic acid, 4,4-dimethyl-3-[[(phenylmethoxy)carbonyl]amino]-, (3S)-
H-Cys(Z)-OH
N-[1-(S)-Benzyloxycarbonyl-3-phenylpropyl]-L-alanine tert-Butyl Ester
2-Chloro-6-(1-hydroxycyclobutyl)benzenemethanol
5-Bromo-3-ethoxybenzofuran-2-carboxylic acid
5-Bromo-3-propoxybenzofuran-2-carboxylic acid
1-[(3-Methyl-3-oxetanyl)methyl]-1H-indazole-6-methanol
1-(Cyclopropylmethyl)-1H-indazole-6-methanol
tert-butyl 2-methyl-1H-pyrrole-3-carboxylate
1-Isobutyl-1H-indazole-4-carboxylic acid methyl ester
2-Chloro-6-(trifluoromethyl)benzyl methanesulfonate
3-Ethyl-4-(methoxycarbonyl)benzoic acid
methyl 3-fluoro-4-(1H-pyrazolo[4,3-b]pyridin-3-yl)benzoate

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