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193201-63-7

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193201-63-7 Usage

Chemical class

Spiro compounds

Explanation

This compound belongs to a class of organic compounds that have two rings connected by a single atom.

Explanation

Due to its spirocyclic structure, this compound may have unique properties and potential biological activities that could be useful in the development of drugs or agrochemical agents.

Explanation

Further studies are needed to understand the compound's properties, such as its chemical reactivity, stability, and potential interactions with biological systems. This research could reveal its suitability as a drug candidate or an agrochemical agent.

Explanation

The specific biological activities of this compound are not yet known, and further research is required to determine its potential as a drug candidate or an agrochemical agent.

Explanation

The chemical formula represents the composition of the compound, indicating the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms present in the molecule.

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule, which can be used to calculate the mass of a specific quantity of the compound.

Explanation

The solubility of the compound in various solvents is not yet known and would need to be determined through experimental studies.

Explanation

The stability of the compound under different conditions, such as temperature, pressure, and exposure to light or moisture, is not yet known and would need to be investigated.

Explanation

The reactivity of the compound with other chemicals or under different conditions is not yet known and would need to be studied to understand its potential applications and limitations.

Unique structure

Spiro ring with a phenylmethyl group at the 7th position

Potential applications

Pharmaceutical and agricultural industries

Research focus

Exploration of properties and potential applications

Biological activities

Unknown at this stage

Molecular weight

Approximately 221.28 g/mol

Solubility

Unknown at this stage

Stability

Unknown at this stage

Reactivity

Unknown at this stage

Check Digit Verification of cas no

The CAS Registry Mumber 193201-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 193201-63:
(8*1)+(7*9)+(6*3)+(5*2)+(4*0)+(3*1)+(2*6)+(1*3)=117
117 % 10 = 7
So 193201-63-7 is a valid CAS Registry Number.

193201-63-7SDS

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 7-benzyl-1,4-dioxa-8-azaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 7-(phenylmethyl)-1,4-dioxa-8-azaspiro[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:193201-63-7 SDS

193201-63-7Relevant articles and documents

A Robust, Recyclable Resin for Decagram Scale Resolution of (±)-Mefloquine and Other Chiral N-Heterocycles

Kreituss, Imants,Chen, Kuang-Yen,Eitel, Simon H.,Adam, Jean-Michel,Wuitschik, Georg,Fettes, Alec,Bode, Jeffrey W.

supporting information, p. 1553 - 1556 (2016/02/12)

Decagram quantities of enantiopure (+)-mefloquine have been produced via kinetic resolution of racemic mefloquine using a ROMP-gel supported chiral acyl hydroxamic acid resolving agent. The requisite monomer was prepared in a few synthetic steps without chromatography and polymerization was safely performed on a >30 gram scale under ambient conditions. The reagent was readily regenerated and reused multiple times for the resolution of 150 grams of (±)-mefloquine and other chiral N-heterocylces.

SUBSTITUTED 1,4-DI-PIPERIDIN-4-YL-PIPERAZINE DERIVATIVES AND THEIR USE AS NEUROKININ ANTAGONISTS

-

Page 32, (2008/06/13)

The invention concerns substituted 1,4-di-piperidin-4-yl-piperazine derivatives having neurokinin antagonistic activity, in particular NK1 antagonistic activity, their preparation, compositions comprising them and their use as a medicine, in particular fo

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