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Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate is a versatile chemical compound utilized in the realm of organic chemistry. It features a carboxybenzyl (Cbz) protecting group, which is crucial for preventing undesired reactions during organic synthesis. Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate is distinguished by its piperidine structure, a prevalent component in pharmaceuticals and natural bioactive compounds, along with its hydroxy and carboxylate groups that enhance its reactivity and the potential for further chemical transformations. The specific physical properties, including melting point, boiling point, and specific rotation, can be ascertained from chemical suppliers or catalogs.

1095010-45-9

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1095010-45-9 Usage

Uses

Used in Organic Synthesis:
Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate is used as a building block or reagent in various synthetic reactions for the development of pharmaceuticals and other organic compounds. Its carboxybenzyl protecting group plays a significant role in shielding functional groups from unwanted reactions, ensuring the successful synthesis of target molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate is used as a key intermediate in the synthesis of various bioactive compounds and drug candidates. Its piperidine structure and functional groups make it a valuable component in the creation of new therapeutic agents with potential medicinal properties.
Used in Research and Development:
Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate is employed as a research tool in academic and industrial laboratories. It aids chemists in exploring novel synthetic pathways, understanding reaction mechanisms, and developing innovative methodologies for the synthesis of complex organic molecules.
Used in Chemical Libraries:
Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate is also utilized in the construction of chemical libraries, which are collections of diverse chemical entities used for high-throughput screening and drug discovery. Its unique structure and reactivity make it a valuable addition to such libraries, contributing to the identification of new lead compounds and potential therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1095010-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,0,1 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1095010-45:
(9*1)+(8*0)+(7*9)+(6*5)+(5*0)+(4*1)+(3*0)+(2*4)+(1*5)=119
119 % 10 = 9
So 1095010-45-9 is a valid CAS Registry Number.

1095010-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 1-Cbz-5-Hydroxypiperidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Benzyl 3-methyl 5-hydroxypiperidine-1,3-dicarboxylate

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:1095010-45-9 SDS

1095010-45-9Relevant academic research and scientific papers

QUINAZOLINE COMPOUNDS, PREPARATION METHODS AND USES THEREOF

-

, (2022/01/12)

Provided herein are novel compounds, for example, compounds having a Formula (I), Formula (II), or Formula (III), or a pharmaceutically acceptable salt thereof. Also provided herein are methods of preparing the compounds and methods of using the compounds, for example, in inhibiting KRAS G12D in a cancer cell, and/or in treating various cancer such as pancreatic cancer, colorectal cancer, lung cancer or endometrial cancer.

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