Cas 3936-30-9,bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)phthalate

3936-30-9

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Basic information

Product Name: bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)phthalate
Synonyms: bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)phthalate
CAS NO:3936-30-9
Molecular Formula:
Molecular Weight: 474.598
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: bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)phthalate(CAS DataBase Reference)
NIST Chemistry Reference: bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)phthalate(3936-30-9)
EPA Substance Registry System: bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)phthalate(3936-30-9)

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: 3936-30-9(Hazardous Substances Data)

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3936-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3936-30-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3936-30:
(6*3)+(5*9)+(4*3)+(3*6)+(2*3)+(1*0)=99
99 % 10 = 9
So 3936-30-9 is a valid CAS Registry Number.

3936-30-9Relevant academic research and scientific papers

A time-resolved electron paramagnetic resonance investigation of the spin exchange and chemical interactions of reactive free radicals with isotopically symmetric (14N-X-14N) and isotopically asymmetric ( 14N-X-15

Sartori, Elena,Khudyakov, Igor V.,Lei, Xuegong,Turro, Nicholas J.

, p. 7785 - 7792 (2007)

Interactions between reactive free radicals (r) with stable mononitroxyl radicals (N) and bisnitroxyl radicals (N-X-N) were studied by time-resolved electron paramagnetic resonance (TR-EPR). Reactive spin-polarized free radicals (r#), with non-

Inhibition of polymerization of unsaturated monomers

-

, (2008/06/13)

Disclosed herein is a method for inhibiting the premature polymerization of ethylenically unsaturated monomers comprising adding to said monomers an effective amount of a mixture comprising: A) at least one stable hindered nitroxyl compound having the structural formula: wherein R1and R4are independently selected from the group consisting of hydrogen, alkyl, and heteroatom-substituted alkyl and R2and R3are independently selected from the group consisting of alkyl and heteroatom-substituted alkyl; and X1and X2(1) are independently selected from the group consisting of halogen, cyano, COOR7, —S—COR7, —OCOR7, (wherein R7is alkyl or aryl), amido, —S—C6H5, carbonyl, alkenyl, or alkyl of 1 to 15 carbon atoms, or (2) taken together, form a ring structure with the nitrogen; and B) at least one inhibitor selected from the group consisting of ortho-quinone, ortho-hydroquinone, para-quinone, para-hydroquinone, and derivatives of the foregoing.