Z-L-phenylalaninol - 98%, high purity , CAS No.6372-14-1

  • ≥98%
Item Number
P117143
Grouped product items
SKUSizeAvailabilityPrice Qty
P117143-1g
1g
In stock
$30.90
P117143-5g
5g
In stock
$81.90
P117143-25g
25g
In stock
$367.90

Basic Description

Synonymsbenzyl N-[(1S)-1-benzyl-2-hydroxy-ethyl]carbamate;(S)-2-(Cbz-amino)-3-phenyl-1-propanol | N-(((benzyl)oxy)-carbony)-L-phenylalaninol | Cbz-L-Phenylalaninol | Z-L-Phenylalaninol, 97% | (S)-2-(Cbz-amino)-3-phenyl-1-propanol | BP-20354 | M03460 | BDBM5013946
Specifications & Purity≥98%
Shipped InNormal
Note25g、1g卖完停产,不再备货

Associated Targets(Human)

CTRB1 Tchem Beta-chymotrypsin (261 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid488191634
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488191634
IUPAC Name benzyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamate
INCHI InChI=1S/C17H19NO3/c19-12-16(11-14-7-3-1-4-8-14)18-17(20)21-13-15-9-5-2-6-10-15/h1-10,16,19H,11-13H2,(H,18,20)/t16-/m0/s1
InChi Key WPOFMMJJCPZPAO-INIZCTEOSA-N
Canonical SMILES C1=CC=C(C=C1)CC(CO)NC(=O)OCC2=CC=CC=C2
Isomeric SMILES C1=CC=C(C=C1)C[C@@H](CO)NC(=O)OCC2=CC=CC=C2
WGK Germany 3
PubChem CID 853481
Molecular Weight 285.34
Beilstein 2816420
Reaxy-Rn 2816420

Certificates

Certificate of Analysis(COA)

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3 results found

Lot NumberCertificate TypeDateItem
L1212064Certificate of AnalysisAug 12, 2024 P117143
D2324748Certificate of AnalysisMay 11, 2023 P117143
D2324754Certificate of AnalysisMay 10, 2023 P117143

Chemical and Physical Properties

Specific Rotation[α]-42 ° (C=2, MeOH)
Melt Point(°C)92-95°C

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 2816420

Related Documents

References

1. D Scholz,A Billich,B Charpiot,P Ettmayer,P Lehr,B Rosenwirth,E Schreiner,H Gstach.  (1994-09-16)  Inhibitors of HIV-1 proteinase containing 2-heterosubstituted 4-amino-3-hydroxy-5-phenylpentanoic acid: synthesis, enzyme inhibition, and antiviral activity..  Journal of medicinal chemistry,  37  ((19)): (3079-3089).  [PMID:7932531]
2. Pierre L. Beaulieu,Dominik Wernic.  (1996-05-31)  Preparation of Aminoalkyl Chlorohydrin Hydrochlorides: Key Building Blocks for Hydroxyethylamine-Based HIV Protease Inhibitors..  The Journal of organic chemistry,  61  ((11)): (3635-3645).  [PMID:11667209]
3. P Y Lam,Y Ru,P K Jadhav,P E Aldrich,G V DeLucca,C J Eyermann,C H Chang,G Emmett,E R Holler,W F Daneker,L Li,P N Confalone,R J McHugh,Q Han,R Li,J A Markwalder,S P Seitz,T R Sharpe,L T Bacheler,M M Rayner,R M Klabe,L Shum,D L Winslow,D M Kornhauser,C N Hodge.  (1996-08-30)  Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas..  Journal of medicinal chemistry,  39  ((18)): (3514-3525).  [PMID:8784449]
4. C N Hodge,P E Aldrich,L T Bacheler,C H Chang,C J Eyermann,S Garber,M Grubb,D A Jackson,P K Jadhav,B Korant,P Y Lam,M B Maurin,J L Meek,M J Otto,M M Rayner,C Reid,T R Sharpe,L Shum,D L Winslow,S Erickson-Viitanen.  (1996-04-01)  Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450..  Chemistry & biology,  ((4)): (301-314).  [PMID:8807858]

Solution Calculators