Cas 1309601-36-2,5'-fluoro-1'-benzyl-4H-spiro[cyclohexa-2,5-diene-1,3'-indol]-2',4(1'H)-dione

1309601-36-2

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Basic information

Product Name: 5'-fluoro-1'-benzyl-4H-spiro[cyclohexa-2,5-diene-1,3'-indol]-2',4(1'H)-dione
Synonyms: 5'-fluoro-1'-benzyl-4H-spiro[cyclohexa-2,5-diene-1,3'-indol]-2',4(1'H)-dione
CAS NO:1309601-36-2
Molecular Formula:
Molecular Weight: 319.335
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: 5'-fluoro-1'-benzyl-4H-spiro[cyclohexa-2,5-diene-1,3'-indol]-2',4(1'H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5'-fluoro-1'-benzyl-4H-spiro[cyclohexa-2,5-diene-1,3'-indol]-2',4(1'H)-dione(1309601-36-2)
EPA Substance Registry System: 5'-fluoro-1'-benzyl-4H-spiro[cyclohexa-2,5-diene-1,3'-indol]-2',4(1'H)-dione(1309601-36-2)

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: 1309601-36-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309601-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,6,0 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1309601-36:
(9*1)+(8*3)+(7*0)+(6*9)+(5*6)+(4*0)+(3*1)+(2*3)+(1*6)=132
132 % 10 = 2
So 1309601-36-2 is a valid CAS Registry Number.

1309601-36-2Upstream product

1309601-39-5 C₂₀H₁₆FNO₂

1309601-36-2Downstream Products

1309601-36-2Relevant academic research and scientific papers

Iodobenzene-mediated intramolecular oxidative coupling of substituted 4-hydroxyphenyl-N-phenylbenzamides for the synthesis of spirooxindoles

Yu, Zhengsen,Ju, Xuhui,Wang, Junyan,Yu, Wei

, p. 860 - 866 (2011)

Phenyliodine(III) bis(trifluoroacetate) (PIFA) can effect the intramolecular oxidative coupling of substituted 4-hydroxyphenyl-N- phenylbenzamides. The transformations could be realized in a catalytic manner by using iodobenzene as catalyst and m-chloro-p

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