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Silane, [(1Z,3Z)-1-bromo-4-(2-bromophenyl)-1,3-butadienyl]trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154467-44-4

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154467-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154467-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,6 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 154467-44:
(8*1)+(7*5)+(6*4)+(5*4)+(4*6)+(3*7)+(2*4)+(1*4)=144
144 % 10 = 4
So 154467-44-4 is a valid CAS Registry Number.

154467-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z,Z)-1-bromo-4-(2-bromophenyl)-1-trimethylsilyl-1,3-butadiene

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 -
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More Details:154467-44-4 SDS

154467-44-4Relevant academic research and scientific papers

A versatile synthesis of 1-benzoheteroepines containing group 14, 15, and 16 heavier elements via a common 1,6-dilithium intermediate

Yasuike, Shuji,Shiratori, Shin-Ichi,Kurita, Jyoji,Tsuchiya, Takashi

, p. 1108 - 1114 (2007/10/03)

Fully unsaturated group 14 (Si, Ge, and Sn), group 15 (P, As, Sb, and Bi) and group 16 (S, Se, and Te) 2-trimethylsilyl-1-benzoheteroepines (16a- j), including the first isolated examples of bismepines, have been prepared by reaction of the corresponding electrophilic metal reagents (MX2 or MX4; M=group 14, 15, and 16 heavier elements) with the key 1,6-dilithium intermediate (9), generated from the common starting compound (Z,Z)-1-bromo- 4-(2-bromophenyl)-1-trimethylsilyl-1,3-butadiene (14) by treatment with tert- butyllithium. The trimethylsilyl group in 16b-j was readily removed by treatment with tetrabutylammonium fluoride to give the desired C- unsubstituted 1-benzoheteroepines (1b-j). Single crystal X-ray analyses of 1d (P) and 1f (Sb) revealed that the seven-membered rings exist in boat conformations with the heteroatoms at the bows. All obtained C-unsubstituted group 15 and 16 1-benzoheteroepines (1d-j) were thermolabile in solution towards heteroatom extrusion, while heteroepines (16d-j) having the bulky trimethylsilyl group at the 2-position were much more stable than 1d-j. The half-lives of 1d-j estimated from 1H-NMR spectral analysis indicate that the thermal stabilities of 1d-j decrease in the order 1f (Sb)>1d (P)>1e (As)>1g (Bi) in the group 15 heteroepines and 1j (Te)>1i (Se)>1h (S) in the group 16 heteroepines.

Synthesis of the Group 15 1-Benzoheteroepines, Dibenzoheteroepines and Dibenzoheteroepines involving the First Isolated Examples of Arsepines and Bismepines

Yasuike, Shuji,Ohta, Hideo,Shiratori, Shinichi,Kurita, Jyoji,Tsuchiya, Takashi

, p. 1817 - 1819 (2007/10/02)

The C-unsubstituted fully unsaturated Group 15 (P, As, Sb and Bi) 1-benzoheteroepines 6, dibenzoheteroepines 8 and dibenzoheteroepines 10 have been prepared from the dibromo compounds 3,7 and 9 having a 1,6-dibromohexatriene system, and their thermal stabilities have been examined.

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