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Silane, dimethyl(phenylmethoxy)-, also known as (dimethylphenylsilyl)oxymethane, is a chemical compound with the molecular formula C9H14OSi. It is a colorless liquid that is soluble in organic solvents and is commonly used as a reagent in organic synthesis, particularly in the formation of silyl ethers and as a protecting group for alcohols. Silane, dimethyl(phenylmethoxy)- is also utilized in the synthesis of various organosilicon compounds and has applications in the electronics and pharmaceutical industries. Due to its reactivity, it should be handled with care, and appropriate safety measures should be taken during its use.

2487-89-0

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2487-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2487-89-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2487-89:
(6*2)+(5*4)+(4*8)+(3*7)+(2*8)+(1*9)=110
110 % 10 = 0
So 2487-89-0 is a valid CAS Registry Number.

2487-89-0SDS

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 dimethyl(phenylmethoxy)silane

1.2 Other means of identification

Product number -
Other names (benzyloxy)dimethylsilane

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:2487-89-0 SDS

2487-89-0Relevant academic research and scientific papers

Hydrosilane-Promoted Facile Deprotection of tert-Butyl Groups in Esters, Ethers, Carbonates, and Carbamates

Ikeda, Takuya,Zhang, Zhenzhong,Motoyama, Yukihiro

supporting information, p. 673 - 677 (2019/01/04)

Combination of PdCl2 with 1,1,3,3-tetramethyldisiloxane in the presence of activated carbon was found to be an effective catalyst system for the cleavage reaction of C?O bond of O?t-Bu moieties. The present catalytic reaction offers a practical method for the deprotection of tert-butyl esters, tert-butyl ethers, O-Boc, and N-Boc derivatives under mild conditions. The addition of activated carbon in the reaction mixture was proved to be crucial for not only sustaining the catalytic activity but also trapping the palladium species after the reaction. (Figure presented.).

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