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Oxaspiropentane is a heterocyclic organic compound characterized by a five-membered ring structure, which includes one oxygen atom and four carbon atoms. It is a spiro compound, meaning it features a spiro junction where two rings share a common carbon atom. Oxaspiro[2.5]octane, a specific example of oxaspiro pentane, is a cyclic ether with the molecular formula C7H12O. Oxaspiropentane is known for its unique structural properties and potential applications in various chemical and pharmaceutical processes. Due to its cyclic nature and the presence of an oxygen atom, oxaspiro pentanes can exhibit interesting reactivity and stability, making them a subject of interest in organic chemistry research.

157-41-5

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157-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157-41-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 157-41:
(5*1)+(4*5)+(3*7)+(2*4)+(1*1)=55
55 % 10 = 5
So 157-41-5 is a valid CAS Registry Number.

157-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oxaspiro[2.2]pentane

1.2 Other means of identification

Product number -
Other names 1-oxa-spiro[2.2]pentane

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:157-41-5 SDS

157-41-5Upstream product

157-41-5Relevant academic research and scientific papers

PYRROLO[2,3-D]PYRIMIDINE TROPOMYOSIN-RELATED KINASE INHIBITORS

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Page/Page column 156, (2014/04/18)

The present invention relates to compounds of Formula (I) and their pharmaceutically acceptable salts, wherein the substituents are as described herein, and their use in medicine, in particular as Trk antagonists.

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