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1331777-74-2

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1331777-74-2 Usage

Description

cis-4-Amino-1-Boc-3-hydroxypiperidine, a chemical compound with the molecular formula C11H21N3O3, is a derivative of piperidine that features an amino group and a Boc (tert-butoxycarbonyl) protecting group. This versatile molecule is widely recognized for its role in organic synthesis, particularly as a building block for the creation of pharmaceuticals and bioactive molecules. The presence of the Boc protecting group enables selective deprotection and further functionalization, enhancing its utility in synthetic chemistry.

Uses

Used in Pharmaceutical Synthesis:
cis-4-Amino-1-Boc-3-hydroxypiperidine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. The Boc protecting group facilitates selective reactions, allowing for the creation of complex molecular structures with precision.
Used in Organic Synthesis:
In the realm of organic synthesis, cis-4-Amino-1-Boc-3-hydroxypiperidine serves as a valuable building block for the preparation of a wide array of bioactive molecules. Its structural features make it suitable for the synthesis of compounds with potential applications in medicine, agriculture, and other fields.
Used in Peptide and Peptide-like Structure Production:
cis-4-Amino-1-Boc-3-hydroxypiperidine is utilized in the production of peptide and peptide-like structures, where its unique properties contribute to the formation of biologically active peptides. The Boc group plays a crucial role in the synthesis process, allowing for the controlled formation of peptide bonds and the subsequent development of peptide-based therapeutics.
Used in Research and Development:
In research and development settings, cis-4-Amino-1-Boc-3-hydroxypiperidine is employed as a model compound for studying the synthesis and properties of various organic and bioactive molecules. Its reactivity and structural features provide insights into the behavior of similar compounds and contribute to the advancement of synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1331777-74-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,1,7,7 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1331777-74:
(9*1)+(8*3)+(7*3)+(6*1)+(5*7)+(4*7)+(3*7)+(2*7)+(1*4)=162
162 % 10 = 2
So 1331777-74-2 is a valid CAS Registry Number.

1331777-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3S,4R)-4-amino-3-hydroxypiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names CIS-4-AMINO-1-BOC-3-HYDROXYPIPERIDINE

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:1331777-74-2 SDS

1331777-74-2Relevant articles and documents

TBK/IKK INHIBITOR COMPOUNDS AND USES THEREOF

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, (2017/01/23)

The present invention relates to compounds of Formula I and pharmaceutically acceptable compositions thereof, useful as TBK/IKKε inhibitors.

PYRROLO[2,3-D]PYRIMIDINYL, PYRROLO[2,3-B]PYRAZINYL AND PYR-ROLO[2,3-D]PYRIDINYL ACRYLAMIDES

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Paragraph 0473, (2015/06/17)

The present invention provides pharmaceutically active pyrrolo[2,3-d]pyrimidinyl and pyrrolo[2,3-d]pyridinyl acrylamides and analogues thereof. Such compounds are useful for inhibiting Janus Kinase (JAK). This invention also is directed to compositions comprising methods for making such compounds, and methods for treating and preventing conditions mediated by JAK.

METHYLPYRROLOPYRIMIDINECARBOXAMIDES

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, (2012/06/18)

The compounds of Formula (I), wherein R1, R2, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiesterase.

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