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1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE is a spirocyclic amine chemical compound with the molecular formula C11H21NO2. It features a bicyclic structure with a nitrogen atom and a tert-butoxycarbonyl (BOC) protecting group attached to one of the nitrogen atoms. 1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE is widely recognized for its role as a building block in organic synthesis and as a reagent in various chemical reactions.

960294-14-8

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960294-14-8 Usage

Uses

Used in Pharmaceutical Industry:
1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE is used as a key component in the synthesis of various bioactive compounds. Its unique structure and reactivity make it a valuable intermediate for the development of new pharmaceutical agents, contributing to the advancement of drug discovery and medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE serves as a crucial building block for the synthesis of agrochemicals, including pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness and selectivity, leading to improved crop protection and agricultural productivity.
Used in Organic Synthesis:
1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE is utilized as a versatile building block in organic synthesis, allowing for the creation of a diverse range of chemical structures. Its spirocyclic amine functionality and BOC protecting group enable selective reactions and the formation of complex molecular architectures, which are essential in the synthesis of specialty chemicals and advanced materials.
Used as a Reagent in Chemical Reactions:
1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE also functions as a reagent in various chemical reactions, facilitating the formation of desired products and improving the efficiency of synthetic processes. Its reactivity and stability under different reaction conditions make it a valuable tool for chemists in both academic and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 960294-14-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,2,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 960294-14:
(8*9)+(7*6)+(6*0)+(5*2)+(4*9)+(3*4)+(2*1)+(1*4)=178
178 % 10 = 8
So 960294-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2O2/c19-15(20-12-14-6-2-1-3-7-14)18-11-5-9-16(13-18)8-4-10-17-16/h1-3,6-7,17H,4-5,8-13H2

960294-14-8SDS

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 tert-butyl 1,9-diazaspiro[4.5]decane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-BOC-1,7-DIAZA-SPIRO[4.5]DECANE

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:960294-14-8 SDS

960294-14-8Downstream Products

960294-14-8Relevant academic research and scientific papers

NITROGEN-CONTAINING SPIROCYCLIC COMPOUNDS AND PHARMACEUTICAL USES THEREOF

-

Page/Page column 57, (2011/06/24)

A compound of the following general formula [I]: wherein each symbol has the same meaning as defined herein, or a pharmaceutically acceptable salt thereof, or a solvate thereof, and a pharmaceutical use of the same in treating organ transplant rejection, graft versus host reaction after transplantation, autoimmune disease, allergic disease and chronic myeloproliferative disease.

Practical synthesis of structurally important spirodiamine templates

Tang,Qu,Xu,Ma,Chen, Shu-Hui,Li

, p. 3793 - 3799 (2008/02/10)

A general, concise, four-step synthetic sequence for the preparation of spirodiamine templates is described herein. Copyright Taylor & Francis Group, LLC.

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