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(E)-1-(2,4,6-triisopropylphenyl)-2-(2,4,6-tri-tert-butylphenyl)diphosphene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87437-16-9

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87437-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87437-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,3 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87437-16:
(7*8)+(6*7)+(5*4)+(4*3)+(3*7)+(2*1)+(1*6)=159
159 % 10 = 9
So 87437-16-9 is a valid CAS Registry Number.

87437-16-9Relevant academic research and scientific papers

SYNTHESIS AND PHOTOREACTIONS OF E-1-(2,4,6-TRIISOPROPYLPHENYL)-2-(2,4,6-TRI-TERT-BUTYLPHENYL)DIPHOSPHENE

Komen, Corine M. D.,Goede, Simon J.,Bickelhaupt, Friedrich

, p. 251 (2007/10/02)

The synthesis and irradiation of the title compound E-1 are discussed.

Synthesis, Photochemical Behaviour and cis/trans Isomerisation of 1-(2,4,6-Triisopropylphenyl)-2-(2,4,6-tri-tert-butylphenyl)diphosphene

Komen, Corine M. D.,Kanter, Frans J. J. de,Goede, Simon J.,Bickelhaupt, Friedrich

, p. 807 - 812 (2007/10/02)

Irradiation of (E)-1-(3,4,6-triisopropylphenyl)-2-(2,4,6-tri-tert-butylphenyl)diphosphene (1a) yields its thermally unstable cis-isomer 1b, the diastereoisomeric cyclisation products 4a and 4b and the cleavage product 5.A mechanism for the formation of these products is proposed.The activation parameters for the thermal isomerisation reaction 1b -> 1a are experimentally determined as ΔH(excit.)=29.5 +/-1.4 kcal mol-1 and ΔS(excit.)=38 +/- 6 cal mol-1 K-1 (1 kcal=4.18 kJ); ΔH(excit.) is the first experimentally determined measure for the strength of the ?-component of a phosphorus-phosphorus double bond.

STABLE UNSYMMETRICAL DIPHOSPHENES

Smit, C.N.,van der Knaap, Th.A.,Bickelhaupt, F.

, p. 2031 - 2034 (2007/10/02)

Variation of the ortho-alkyl substituents in diaryldiphosphenes revealed that their stability is determined by steric hindrance.By suitable combinations of ortho-substituents, it was therefore possible to prepare the first relatively stable unsymmetrical

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