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89288-22-2

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89288-22-2 Usage

Description

(S)-2-AMino-3-(4-nitrophenyl)propanol is a chiral organic compound with the molecular formula C9H11NO3. It is characterized by the presence of an amino group (-NH2) at the 2nd carbon, a 4-nitrophenyl group attached to the 3rd carbon, and a hydroxyl group (-OH) at the same 3rd carbon. The "S" configuration indicates that the molecule has a specific three-dimensional arrangement of these functional groups, which is crucial for its properties and applications.

Uses

Used in Pharmaceutical Industry:
(S)-2-AMino-3-(4-nitrophenyl)propanol is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to serve as a building block for the development of new drugs with potential therapeutic applications.
Used in the Synthesis of 2-Substituted Thiazole Carboxamides:
In the field of medicinal chemistry, (S)-2-AMino-3-(4-nitrophenyl)propanol is utilized in the preparation of a new series of 2-substituted thiazole carboxamides. These compounds have been identified as potent inhibitors of Akt kinases, which are important targets for the treatment of various diseases, including cancer and metabolic disorders. By inhibiting Akt kinases, these thiazole carboxamides can modulate cellular signaling pathways and potentially lead to the development of effective therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 89288-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,8 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89288-22:
(7*8)+(6*9)+(5*2)+(4*8)+(3*8)+(2*2)+(1*2)=182
182 % 10 = 2
So 89288-22-2 is a valid CAS Registry Number.

89288-22-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-(4-nitrophenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names 4-nitro-L-phenylalaninol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89288-22-2 SDS

89288-22-2Relevant articles and documents

Synthesis of Water-Soluble Chiral DOTA Lanthanide Complexes with Predominantly Twisted Square Antiprism Isomers and Circularly Polarized Luminescence

Dai, Lixiong,Zhang, Junhui,Chen, Yuqing,Mackenzie, Lewis E.,Pal, Robert,Law, Ga-Lai

supporting information, p. 12506 - 12510 (2019/10/02)

One-step cyclization of a tetraazamacrocycle 5 with 70% yield in a 25-g scale was performed. Its chiral DOTA derivatives, L4, has ?93% of TSAP coordination isomer in its Eu(III) and Yb(III) complexes in aqueous solution. [GdL4]5- exhibits a high relaxivity, making it a promising and efficient MRI contrast agent. High luminescence dissymmetry factor (glum) values of 0.285 (ΔJ = 1) for [TbL3]- and 0.241 (ΔJ = 1) for [TbL4]5- in buffer solutions were recorded.

ANTIBODY DRUG CONJUGATES

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, (2017/01/02)

This application discloses anti-P-cadherin antibodies, antigen binding fragments thereof, and antibody drug conjugates of said antibodies or antigen binding fragments, particularly antibody drug conjugates comprising anti-P-cadherin antibodies conjugated to auristatin analogs. The invention also relates to methods of treating cancer using the antibody drug conjugates. Also disclosed herein are methods of making the antibodies, antigen binding fragments, and antibody drug conjugates, and methods of using the antibodies and antigen binding fragments as diagnostic reagents.

COMPOUNDS FOR POSITRON EMISSION TOMOGRAPHY

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Paragraph 0373-0375, (2016/12/26)

Described herein are compounds, compositions, and methods for diagnosing and/or monitoring pathogenic disease using positron emission tomography. Also described are conjugates of the formula B-L-P, wherein B is a radical of a targeting agent selected from vitamin receptor binding ligands (such as folate), PSMA binding ligands, or PSMA inhibitors; L is a divalent linker comprising aspartic acid, lysine, or arginine, and P is a radical of an imaging agent or radiotherapy agent, such as a radionuclide or radionuclide containing group, or a radical of a compound capable of binding a radionuclide, such as a metal chelating group.

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