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140645-22-3

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140645-22-3 Usage

Description

(S)-Tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate is a chemical compound derived from piperidine, featuring an azide functional group and a tert-butyl group. (S)-Tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate is utilized in organic synthesis and medicinal chemistry due to its unique structural characteristics and reactivity.

Uses

Used in Organic Synthesis:
(S)-Tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate is used as a synthetic intermediate for the preparation of various piperidine derivatives. Its azide functional group allows for click chemistry reactions, which are valuable in creating complex molecular structures with high efficiency and selectivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-Tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate serves as a building block for the synthesis of biologically active compounds. Its structural features may contribute to potential pharmacological applications, making it a valuable tool for drug discovery and development.
Used in Chemical Biology Research:
Additionally, (S)-Tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate can be employed as a research tool in chemical biology. Its unique properties and reactivity make it suitable for exploring new chemical reactions and understanding the interactions between molecules at a fundamental level.
Overall, (S)-Tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate has a wide range of applications across different industries, including organic synthesis, medicinal chemistry, and chemical biology research, due to its versatile chemical properties and potential for creating novel compounds with biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 140645-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,4 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 140645-22:
(8*1)+(7*4)+(6*0)+(5*6)+(4*4)+(3*5)+(2*2)+(1*2)=103
103 % 10 = 3
So 140645-22-3 is a valid CAS Registry Number.

140645-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3S)-3-(azidomethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (3S)-3-azidomethyl-1-(tert-butoxycarbonyl)-piperidine

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:140645-22-3 SDS

140645-22-3Relevant articles and documents

INDOLE DERIVATIVES AND USES THEREOF FOR TREATING A CANCER

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Page/Page column 71; 85; 88; 113-114, (2022/02/06)

The present invention relates to indole derivatives of formula (I') as CK2 inhibitor and pharmaceutical compositions comprising the same. The present invention further relates to the use of such compounds of formula (I) for use for preventing and/or treating a cancer.

NOVEL TRIAZOLOPYRAZINE DERIVATIVE AND USE THEREOF

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, (2015/10/06)

The present invention relates to a novel triazolopyrazine derivative or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition containing the same as an active ingredient for preventing or treating hyper proliferative disorder. The present invention can be useful as a therapeutic agent for various hyper proliferative disorders associated with excessive cell proliferation and growth caused by abnormal kinase activity, such as cancer, psoriasis, rheumatoid arthritis, and diabetic retinopathy, by efficiently inhibiting c-Met tyrosine kinase activity.

Design and synthesis of potent and highly selective thrombin inhibitors

Hilpert,Ackermann,Banner,Gast,Gubernator,Hadvary,Labler,Muller,Schmid,Tschopp,Van de Waterbeemd

, p. 3889 - 3901 (2007/10/02)

Thrombin, a serine protease, plays a central role in the initiation and propagation of thrombotic events. An extensive search for new thrombin inhibitors was performed, using an unconventional approach. Screening of small basic molecules for binding in th

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