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Silanecarbonitrile, triethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18301-88-7

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18301-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18301-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,0 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18301-88:
(7*1)+(6*8)+(5*3)+(4*0)+(3*1)+(2*8)+(1*8)=97
97 % 10 = 7
So 18301-88-7 is a valid CAS Registry Number.

18301-88-7SDS

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 triethylsilylformonitrile

1.2 Other means of identification

Product number -
Other names cyanotriethylsilane

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:18301-88-7 SDS

18301-88-7Relevant academic research and scientific papers

Catalytic C-C bond cleavage and C-Si bond formation in the reaction of RCN with Et3SiH promoted by an iron complex

Nakazawa, Hiroshi,Kamata, Kouji,Itazaki, Masumi

, p. 4004 - 4006 (2007/10/03)

Catalytic C-C bond cleavage of acetonitrile and C-Si bond formation have been attained in the photoreaction of MeCN with Et3SiH in the presence of an iron complex, Cp(CO)2FeMe. This catalytic system can be applied for arylnitrile C-C

Trimethylsilyl Cyanide - A Reagent for Umpolung, V. Nucleophilic Acylation of Alkylating Reagents with α,β-Unsaturated Aldehydes.

Hertenstein, Ulrich,Huenig, Siegfried,Oeller, Manfred

, p. 3783 - 3802 (2007/10/02)

The readily accessible adducts 3 from α,β-unsaturated aldehydes and trimethylsilyl cyanide react smoothly after deprotonation (LDA) as anions 3A with different alkylating agents in 1-position.Removal of the protective group under mild conditions yields the α,β-unsaturated ketones 5 in 60 - 80 percent overall yield.The stability of anions 3A is increased by an O-triethylsilyl group.Alkylation of 3A in 3-position (partly) is caused by 3-acceptor substituents.Nucleophilic acylation with α-alkoxyaldehydes produces 1,2-diketones via a new route.

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