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3-Amino-3-(1-Boc-4-piperidyl)propanoic Acid is a chemical compound categorized under amino acids, characterized by its amino group, a Boc-protected piperidine ring, and a propanoic acid moiety. The Boc (tert-butyloxycarbonyl) protecting group is a key feature that shields the amino group from unwanted reactions during synthetic processes, making it a valuable building block in the synthesis of peptides and other bioactive molecules. Its versatility and potential in the production of biologically active compounds have established its importance in organic synthesis and drug development.

372144-02-0

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372144-02-0 Usage

Uses

Used in Organic Synthesis:
3-Amino-3-(1-Boc-4-piperidyl)propanoic Acid is used as a versatile intermediate for the synthesis of a variety of organic compounds. Its unique structure allows for the creation of complex molecules that can be tailored for specific applications.
Used in Drug Development:
In the pharmaceutical industry, 3-Amino-3-(1-Boc-4-piperidyl)propanoic Acid is utilized as a key component in the development of new drugs. Its role in the synthesis of bioactive molecules contributes to the discovery and creation of innovative therapeutic agents.
Used in Peptide Synthesis:
3-Amino-3-(1-Boc-4-piperidyl)propanoic Acid is employed as a building block in peptide synthesis, where it can be incorporated into peptide sequences to create novel peptide-based drugs or other bioactive peptides.
Used in the Production of Biologically Active Compounds:
Due to its potential as a versatile intermediate, 3-Amino-3-(1-Boc-4-piperidyl)propanoic Acid is used in the production of biologically active compounds that can have various applications in medicine, agriculture, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 372144-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,1,4 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 372144-02:
(8*3)+(7*7)+(6*2)+(5*1)+(4*4)+(3*4)+(2*0)+(1*2)=120
120 % 10 = 0
So 372144-02-0 is a valid CAS Registry Number.

372144-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]piperidin-4-yl]propanoic acid

1.2 Other means of identification

Product number -
Other names -

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:372144-02-0 SDS

372144-02-0Downstream Products

372144-02-0Relevant articles and documents

Piperidine compound and preparation method thereof

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Paragraph 0023; 0032, (2017/03/14)

The invention relates to a piperidine compound and a preparation method thereof. The compound is N-BOC-4-(1-amino-3-hydroxypropenyl) piperidine, and 4-piperidine methanol is used as a staring material, and the compound is synthesized through reactions in six steps, is an important intermediate for preparing a kinase inhibitor and has wide application prospects in preparing medicine for preventing and treating diabetes. The preparation method has the advantages of cheap raw materials and easiness in obtaining the raw materials, and a synthetic method is simple, is a novel method for synthesizing the piperidine compound and is suitable for large-scale industrial production.

2-CYANOPYRROLES AND THEIR ANALOGUES AS DDP-IV INHIBITORS

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Page/Page column 53, (2010/02/08)

The present invention relates to therapeutically active and selective inhibitors of the enzyme DPP-IV having the formula I: (I) The invention furthermore relates to pharmaceutical compositions comprising the compounds and the use of such compounds for the manufacture of medicaments for treating diseases that are associated with proteins which are subject to inactivation by DPP-IV, such as type 2 diabetes and obesity.

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