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Diselenide, bis[[2,4,6-tris(1,1-dimethylethyl)phenyl]methyl] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102737-64-4

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102737-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102737-64-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,3 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102737-64:
(8*1)+(7*0)+(6*2)+(5*7)+(4*3)+(3*7)+(2*6)+(1*4)=104
104 % 10 = 4
So 102737-64-4 is a valid CAS Registry Number.

102737-64-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(2,4,6-tri-tert-butylbenzyl)diselane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102737-64-4 SDS

102737-64-4Downstream Products

102737-64-4Relevant academic research and scientific papers

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.

Reactions of 2,4,6-Tri-t-butylphenyllithium with Deuterated Formate, Thioformate and Selenoformate

Ishii, Akihiko,Okazaki, Renji,Inamoto, Naoki

, p. 1037 - 1040 (2007/10/02)

O-Cholesteryl chalcogenoformates-d, DC(=X)(OR) (2: X=O; 3: X=S; 4: X=Se; R=3β-cholesteryl), were synthesized and allowed to react with 2,4,6-tri-t-butylphenyllithium. 1,3,5-Tri-t-butylbenzene was a main product in each reaction. The other products were 2,4,6-tri-t-butylbenzaldehyde-d (9) for 2, 2,4,6-tri-t-butylthiobenzaldehyde-d for 3, and 9, 6,8-di-t-butyl-1-deuterio-3,4-dihydro-4,4-dimethyl-1H-2-benzoselenin, bis(2,4,6-tri-t-butyl-α-deuteriobenzyl) diselenide, and bis(2,4,6-tri-t-butyl-α-deuteriobenzyl) triselenide for 4.The mechanisms for these reactions have been discussed.

Reactions of 2,4,6-Tri-t-butylphenyllithium with O-Alkyl Selenoformates: Intermediate Formation of 2,4,6-Tri-t-butylselenobenzaldehyde

Ishi, Akihiko,Okazaki, Renji,Inamoto, Naoki

, p. 2529 - 2536 (2007/10/02)

2,4,6-Tri-t-butylphenyllithium reacts with O-alkyl selenoformates (1) at three different sites (i.e., the selenoformyl carbon, the selenoformyl hydrogen, and the selenium) to give 1,3,5-tri-t-butylbenzene, 2,4,6-tri-t-butylbenzaldehyde, 6,8-di-t-butyl-3,4-dihydro-4,4-dimethyl-1H-2-benzoselenin (11), bis(2,4,6-tri-t-butylphenylmethyl) di(and tri) selenides, bis(2,4,6-tri-t-butylphenyl) diselenide, and dibutyl diselenide depending on the reaction conditions and the alkyl group in 1.The formation of 11 is explained in terms of the intermediacy of 2,4,6-tri-t-butylselenobenzaldehyde, which is trapped by condensation rection with butylamine leading to N-(2,4,6-tri-t-butylbenzylidene)butylamine.Mechanism for the formation of these products is also discussed.

Abnormal Reaction of 2,4,6-Tri-t-butylphenyl-lithium with Selenoformates: Possible Intermediacy of Selenobenzaldehyde

Okazaki, Renji,Ishii, Akihiko,Inamoto, Naoki

, p. 71 - 72 (2007/10/02)

The title reaction afforded some products strongly suggestive of the intermediacy of 2,4,6-tri-t-butylselenobenzaldehyde.

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