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36954-58-2

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36954-58-2 Usage

Physical state

Colorless liquid at room temperature

Uses

a. Building block in the synthesis of various organic compounds
b. Fluorinated monomer in the development of advanced materials

Properties

a. High thermal stability
b. Chemical inertness

Unique properties in advanced materials

high resistance to heat, chemicals, and weathering

Environmental considerations

Proper handling and disposal to minimize environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 36954-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,5 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36954-58:
(7*3)+(6*6)+(5*9)+(4*5)+(3*4)+(2*5)+(1*8)=152
152 % 10 = 2
So 36954-58-2 is a valid CAS Registry Number.

36954-58-2Relevant articles and documents

-

Feast,W.J.,Preston,W.E.

, p. 2805 - 2812 (1972)

-

The high-temperature alicyclic ring contraction of 1,1-dichloroperfluorotetralin and the alicyclic ring opening of 1,1-dichloroperfluorobenzocyclobutene

Karpov, Victor M.,Mezhenkova, Tatyana V.,Platonov, Vyacheslav E.

, p. 714 - 717 (2008/03/13)

The pyrolysis of 1,1-dichloroperfluorotetralin (4) in a stream of argon gives a mixture contained perfluoro-1-methyleneindan (1), perfluoro-3-methylindene (6), 1,1-dichloroperfluoroindan (2) and perfluoroindene (7), while copyrolysis of tetralin 4 with CH

THERMOLYTIC REACTIONS OF POLYFLUOROORGANIC COMPOUNDS, PART XXVII. INTERACTION OF 1,1-DICHLOROPOLYFLUOROINDANES WITH HALOFORMS

Karpov, V. M.,Platonov, V. E.,Chuikov, I. P.,Yakobson, G. G.

, p. 459 - 474 (2007/10/02)

A number of polyfluoro-1-methyleneindanes have been obtained by copyrolysis of 1,1-dichloropolyfluoroindanes with CF2=CF2, CHClF2, CHCl2F, CHCl3.A possibility is shown for the reaction of 1,1-dichloroctafluoroindan with CHClF2 to proceed by way of difluorocarbene insertion into the C - Cl bond of the benzylic position of this indan, with subsequent dechlorination of the insertion product.

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