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2,2',4,4',6,6'-hexa-tert-butylstilbene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121654-29-3

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121654-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121654-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121654-29:
(8*1)+(7*2)+(6*1)+(5*6)+(4*5)+(3*4)+(2*2)+(1*9)=103
103 % 10 = 3
So 121654-29-3 is a valid CAS Registry Number.

121654-29-3Downstream Products

121654-29-3Relevant academic research and scientific papers

2-(2,4-Di-tert-butylphenyl)-1,1-bis(trimethylsilyl)silene and 2-(2,4,6-Tri-tert-butylphenyl)-1,1-bis(trimethylslyl)silene - Two new sterically protected but still unstable silaethenes

Luderer, Frank,Retake, Helmut,Oehme, Harfmut

, p. 15 - 20 (1996)

(2,4-Di-terl-butylphenyl)tris(trimethylsilyl)silylmethanol (1a), prepared by the reaction of tris(trimethylsilyl)silylmagnesium bromide with 2,4-di-tert-butylbenzaldehyde, was deprotonated by treatment with methyllithium in ether at -78°C to give the transient 2-(2,4-di-tert-butylphenyi)-1,1-bis(trimethylsilyljsilene (3a), which dimerizes in a head-to-head fashion with the formation of (E)-/(Z)-3,4-bis(2,4-di-terf-butylphenyl)-1,1,2,2-tetrakis(trimethylsilyl)-l,2- disilacyclobutane (5). Besides 5 an unstable compound 4 was obtained, which was preliminarly assigned as 5,7-di-terf-butyl-l-(2,4-di-fert-butylphenyl)-1,2,3,8a-tetrahydro-2,2,3,3- tetrakis(trime thylsilyl)-1,2-disilanaphthalene (4), the formal [2 + 4] cyclodi-mer of 3a. Compound 4 gradually decomposes to give (E)-/(Z)-5, and is considered to be the kinetically preferred dirner of 3a, which is converted into the thermodynamically stable 5. 2,4,6-Tri-tert-butylbenzaldehyde reacts with tris(trimethylsilyljsilyllithium resulting in the formation of 6,8-ditert-butyl-l,2,3,4-tetrahydro-4,4-dimethyl-2,2-bis(trimethylsilyl)-2- silanaphthalene (6). Compound 6 is the product of the insertion of the Si=C bond into the C-H bond of an o-tertbutyl group of the intermediate 2-(2,4,6-tri-ferf-butylphenyl)l,l-bis{t.rimethylsilyl)silene (3b), which despite extreme steric shielding proved to be still unstable. For compounds (Z)-5 and 6 the results of the X-ray analyses are given.

NEW ASPECTS OF ORGANOSELENIUM COMPOUNDS CONTAINING GROUP 14 ELEMENTS

Okazaki, Renji,Tokitoh, Norihiro,Ishii, Akihiko,Ishii, Naoko,Matsuhashi, Yasusuke,et al.

, p. 49 - 66 (2007/10/02)

The synthesis and reactivities of double bond compounds between Group 14 and Group 16 elements have been reported.Specifically the chemistry of M=X type compounds (C=Se, Ge=S, Sn=S, Sn=Se) are described.

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