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Disilane, pentamethyl(1-phenylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61244-94-8

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61244-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61244-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,4 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61244-94:
(7*6)+(6*1)+(5*2)+(4*4)+(3*4)+(2*9)+(1*4)=108
108 % 10 = 8
So 61244-94-8 is a valid CAS Registry Number.

61244-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-(1-phenylethenyl)-trimethylsilylsilane

1.2 Other means of identification

Product number -
Other names 1-Phenylaethenylpentamethyldisilan

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:61244-94-8 SDS

61244-94-8Relevant academic research and scientific papers

CHEMISTRY OF ORGANOSILICON COMPOUNDS. CXXIII. NEW PHOTOCHEMICAL AND THERMAL DEGRADATION REACTIONS OF VINYLDISILANES TO VINYLSILANES THROUGH (η3-1-SILAPROPENYL)TRICARBONYLIRON COMPLEXES

Sakurai, Hideki,Kamiyama, Yoshiyasu,Nakadaira, Yasuhiro

, p. 13 - 30 (1980)

Vinyldisilanes (II) of the type R1CH=CR2SiMe2SiMe3 (a, R1 = Ph, R2 = H; b, R1 = H, R2 = Me; c, R1 = R2 = H) and (R1CH = CHSiMeR3-)2 (d, R1 = Ph, R3 = Me; e, R1 = H, R3 = Ph) undergo a novel degradation reaction to give the corresponding vinylsilanes, R1CH = CR2SiMe3 and (R1CH=CH)2SiMeR3, respectively, under photochemical or thermal conditions in the presence of a stoichiometric amount of pentacarbonyliron.Two α-styryldisilanes (IIf, CH2=CPhSiMe2SiMe3 and IIg, 2) undergo similar degradation reactions, but gave β-styryl- silanes.In the presence of additional benzophenone, IIb, IIc, and IIf gave (E)-Me3SiCH=CRSiMe2OCHPh2 (b, R = Me; c, R = H; f, R = Ph) under either photochemical or thermal conditions, but IIa gave under photochemical, or Ph2CHSiMe3 under thermal conditions as main product.Mechanisms involving η3-1-silapropenyltricarbonyliron intermediates are proposed, and indeed separately prepared (η3-1-silapropenyl)(trimethylsilyl)tricarbonyliron gave the same products under similar conditions.

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