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Disilane, 1,2-dichloro-1,1,2,2-tetrakis(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55642-25-6

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55642-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55642-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,4 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55642-25:
(7*5)+(6*5)+(5*6)+(4*4)+(3*2)+(2*2)+(1*5)=126
126 % 10 = 6
So 55642-25-6 is a valid CAS Registry Number.

55642-25-6SDS

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 chloro-[chloro-di(propan-2-yl)silyl]-di(propan-2-yl)silane

1.2 Other means of identification

Product number -
Other names 1,2-dichloro-1,1,2,2-tetraisopropyldisilane

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:55642-25-6 SDS

55642-25-6Upstream product

55642-25-6Downstream Products

55642-25-6Relevant academic research and scientific papers

Dibenzo[b,e]-7,7,8,8-tetraneopentyl- and dibenzo[b,e]-7,7,8,8-tetraisopropyl-7,8-disilabicyclo[2.2.2]octa-2,5-dienes: Interaction with tetracyanoethylene and transition metal chlorides

Kyushin, Soichiro,Ikarugi, Masanobu,Takatsuna, Kazutoshi,Goto, Midori,Matsumoto, Hideyuki

, p. 121 - 133 (2007/10/03)

Dibenzo[b,e]-7,7,8,8-tetraalkyl-7,8-disilabicyclo[2.2.2]octa-2,5-dienes (1: R = tBuCH2; 2: R = iPr) were prepared by the reaction of ClR2SiSiR2Cl with lithium anthracenide in 1,2-dimethoxyethane (DME) at room temperature. The structure of 1 was determined by X-ray crystallography. Crystal data for 1: monoclinic, C2/c, a = 12.941(2), b = 14.601(1), c = 35.109(6) A, β = 94.957(7)°, V = 6609(2) A3, Z = 8, R = 0.048, Rw = 0.053 for 4037 reflections. Compounds 1 and 2 show the bathochromic shift of 1La and 1Lb bands in UV spectra and exhibit considerably low oxidation potentials due to effective σ-π conjugation. Compounds 1 and 2 form charge-transfer complexes with tetracyanoethylene (TCNE). In the case of 1, the charge-transfer complex (1: TCNE = 2:1) could be isolated as crystals and the structure was determined by X-ray crystallography. Crystal data for the 1-TCNE complex: monoclinic, C2/c, a = 10.267(2), b = 36.077(4), c = 20.022(4) A, β = 100.680(8)°, V = 7288(2) A3, Z = 4, R = 0.045, Rw - 0.077 for 4120 reflections. The action of transition metal chlorides on 2 resulted in [4 + 2] cycloreversion to form CliPr2SiSiiPr2Cl and anthracene.

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