Cas 1335106-39-2,6-bromo-3-iodo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione

1335106-39-2

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Basic information

Product Name: 6-bromo-3-iodo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione
Synonyms: 6-bromo-3-iodo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione
CAS NO:1335106-39-2
Molecular Formula:
Molecular Weight: 442.05
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: 6-bromo-3-iodo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione(CAS DataBase Reference)
NIST Chemistry Reference: 6-bromo-3-iodo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione(1335106-39-2)
EPA Substance Registry System: 6-bromo-3-iodo-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione(1335106-39-2)

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: 1335106-39-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1335106-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,1,0 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1335106-39:
(9*1)+(8*3)+(7*3)+(6*5)+(5*1)+(4*0)+(3*6)+(2*3)+(1*9)=122
122 % 10 = 2
So 1335106-39-2 is a valid CAS Registry Number.

1335106-39-2Upstream product

898138-80-2 N-(2-bromophenyl)-3-phenylpropiolamide

1335106-39-2Downstream Products

1335106-39-2Relevant academic research and scientific papers

Iodocyclization of N-aryl-3-phenylpropiolamides by I2/CAN: A convenient route for the selective synthesis of quinolin-2-ones

Likhar, Pravin R.,Racharlawar, Shailesh S.,Karkhelikar, Manjusha V.,Subhas,Sridhar

experimental part, p. 2407 - 2414 (2011/09/19)

A general method has been developed for the selective synthesis of 3-iodoquinolin-2-ones and spiro[4.5]trienes via intramolecular iodocyclization of N-(ortho-substituted aryl)-3-phenylpropiolamides using iodine/cerium(IV) ammonium nitrate reagent under mi

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