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Benzonitrile, 2-(tributylstannyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79048-34-3

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79048-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79048-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,4 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79048-34:
(7*7)+(6*9)+(5*0)+(4*4)+(3*8)+(2*3)+(1*4)=153
153 % 10 = 3
So 79048-34-3 is a valid CAS Registry Number.

79048-34-3SDS

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 2-tributylstannylbenzonitrile

1.2 Other means of identification

Product number -
Other names o-cyanophenyltributyltin

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:79048-34-3 SDS

79048-34-3Downstream Products

79048-34-3Relevant academic research and scientific papers

Illuminating Stannylation

Sakamoto, Kyoka,Nagashima, Yuki,Wang, Chao,Miyamoto, Kazunori,Tanaka, Ken,Uchiyama, Masanobu

supporting information, p. 5629 - 5635 (2021/05/04)

We have developed photoboosted stannylation reactions of terminal alkynes (linear-selective hydrostannylation) and fluoroarenes (defluorostannylation), in which the stannyl anion is photoexcited to an excited triplet (T1) stannyl diradical species. This u

Generation and reaction of cyano-substituted aryllithium compounds using microreactors

Nagaki, Aiichiro,Kim, Heejin,Usutani, Hirotsugu,Matsuo, Chika,Yoshida, Jun-Ichi

, p. 1212 - 1217 (2010/06/13)

We developed a microflow method for the generation and reactions of aryllithiums bearing a cyano group, including o-lithiobenzonitrile, m-lithiobenzonitrile and p-lithiobenzonitrile. The method was effective at much higher temperatures than are required for conventional macrobatch reactions, by virtue of rapid mixing, short residence time, and efficient temperature control. In addition, reactions of o-lithiobenzonitrile with carbonyl compounds followed by trapping of the resulting lithium alkoxides with electrophiles were achieved in an integrated microflow system. The Royal Society of Chemistry.

New and simple one-step cobalt-catalyzed preparation of functionalized arylstannanes from the corresponding aryl bromides or iodides

Gosmini, Corinne,Perichon, Jacques

, p. 216 - 217 (2007/10/03)

The process for the preparation of functionalized arylstannanes from the corresponding aryl bromides or iodides was described. The corresponding arylstannane was detected by gas chromatography using an internal standard alkane. The two-step coupling react

Palladium-iminophosphine-catalyzed homocoupling of alkynylstannanes and other organostannanes using allyl acetate or air as an oxidant

Shirakawa, Eiji,Nakao, Yoshiaki,Murota, Yasubumi,Hiyama, Tamejiro

, p. 132 - 136 (2007/10/03)

A palladium-iminophosphine complex was found to catalyze the homocoupling reaction of alkynylstannanes using allyl acetate as an oxidant, whereas aryl- and alkenylstannanes were oxidatively homocoupled with air.

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