Cas 1454790-06-7,(E)-1'-acetyl-3-benzylidene-2',4-dioxospiro[cyclopentane-1,3'-indoline]-2,2-dicarbonitrile

1454790-06-7

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Basic information

Product Name: (E)-1'-acetyl-3-benzylidene-2',4-dioxospiro[cyclopentane-1,3'-indoline]-2,2-dicarbonitrile
Synonyms: (E)-1'-acetyl-3-benzylidene-2',4-dioxospiro[cyclopentane-1,3'-indoline]-2,2-dicarbonitrile
CAS NO:1454790-06-7
Molecular Formula:
Molecular Weight: 381.39
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (E)-1'-acetyl-3-benzylidene-2',4-dioxospiro[cyclopentane-1,3'-indoline]-2,2-dicarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1'-acetyl-3-benzylidene-2',4-dioxospiro[cyclopentane-1,3'-indoline]-2,2-dicarbonitrile(1454790-06-7)
EPA Substance Registry System: (E)-1'-acetyl-3-benzylidene-2',4-dioxospiro[cyclopentane-1,3'-indoline]-2,2-dicarbonitrile(1454790-06-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1454790-06-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454790-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,7,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1454790-06:
(9*1)+(8*4)+(7*5)+(6*4)+(5*7)+(4*9)+(3*0)+(2*0)+(1*6)=177
177 % 10 = 7
So 1454790-06-7 is a valid CAS Registry Number.

1454790-06-7Upstream product

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1454790-06-7Relevant academic research and scientific papers

Stereoselective synthesis of five-membered spirooxindoles through Tomita zipper cyclization

Ramachary,Venkaiah, Chintalapudi,Krishna, Patoju M.

, p. 4714 - 4717 (2013)

Functionalized five-membered spirooxindoles were furnished in good yields and excellent stereoselectivities by using an effective Tomita zipper cyclization (TZC) reaction through organophosphine catalysis.

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