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79421-40-2

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79421-40-2 Usage

General Description

4-(1,4-DIOXA-8-AZASPIRO[4.5]DEC-8-YL)BENZENECARBALDEHYDE is a chemical compound that belongs to the class of aldehydes, with the molecular formula C15H17NO3. It is a derivative of benzaldehyde and contains a spiro ring with a dioxane ring and an azaspiro ring attached. 4-(1,4-DIOXA-8-AZASPIRO[4.5]DEC-8-YL)BENZENECARBALDEHYDE is used in the field of organic synthesis and pharmaceutical research. It may have potential applications in the development of drugs and pharmaceutical products due to its unique chemical structure. Further research is required to determine the specific uses and properties of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 79421-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79421-40:
(7*7)+(6*9)+(5*4)+(4*2)+(3*1)+(2*4)+(1*0)=142
142 % 10 = 2
So 79421-40-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO3/c16-11-12-1-3-13(4-2-12)15-7-5-14(6-8-15)17-9-10-18-14/h1-4,11H,5-10H2

79421-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)benzaldehyde

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:79421-40-2 SDS

79421-40-2Relevant articles and documents

An improved synthesis of N-aryl and N-heteroaryl substituted piperidones

Sch?n, Uwe,Messinger, Josef,Buckendahl,Prabhu,Konda

, p. 2519 - 2525 (2008/02/02)

An efficient Pd(0)-catalyzed protocol for the rapid and efficient preparation of N-aryl and N-heteroaryl substituted piperidones is described. The two step syntheses proceed with an overall yield of 50-70% using X-Phos as optimal ligand for the Pd(0)-cata

Cardiotonic agents. 5. 1,2-Dihydro-5-[4-(1H-imidazol-1-yl)phenyl]-6-methyl-2-oxo-3- pyridinecarbonitriles and related compounds. Synthesis and inotropic activity

Sircar,Duell,Bristol,Weishaar,Evans

, p. 1023 - 1029 (2007/10/02)

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