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M-Tolyltrimethylstannane, also known as 3-methylphenyltrimethylstannane or (3-methylphenyl)trimethylstannane, is an organostannane compound with the chemical formula C10H14Sn. It is a colorless liquid that is sensitive to air and moisture, and it is commonly used as a reagent in organic synthesis, particularly in cross-coupling reactions. The compound consists of a trimethylstannyl group (-Sn(CH3)3) attached to a m-tolyl group (3-methylphenyl), which provides it with unique reactivity and selectivity in various chemical transformations. M-Tolyltrimethylstannane is often used in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals, due to its ability to form stable intermediates and facilitate the formation of carbon-carbon bonds.

937-01-9

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937-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 937-01-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 937-01:
(5*9)+(4*3)+(3*7)+(2*0)+(1*1)=79
79 % 10 = 9
So 937-01-9 is a valid CAS Registry Number.

937-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(3-methylphenyl)stannane

1.2 Other means of identification

Product number -
Other names Stannane,trimethyl-m-tolyl

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:937-01-9 SDS

937-01-9Relevant academic research and scientific papers

Visible-Light-Driven Synthesis of Arylstannanes from Arylazo Sulfones

Lian, Chang,Yue, Guanglu,Mao, Jinshan,Liu, Danyang,Ding, Yi,Liu, Zerong,Qiu, Di,Zhao, Xia,Lu, Kui,Fagnoni, Maurizio,Protti, Stefano

supporting information, p. 5187 - 5191 (2019/07/03)

The visible-light-driven preparation of (hetero)aryl stannanes was carried out under both photocatalyst- and metal-free conditions via irradiation of arylazo sulfones in the presence of hexaalkyldistannanes. The reaction shows a high efficiency and a wide substrates scope. The resulting crude organotin derivatives can be directly employed in a Stille protocol.

Synthesis of 1,3,5-tri- and 1,2,4,5-tetrasubstituted tin and mercury derivatives of benzene. Crystal structure of 1,3,5-tris(chloromercurio)benzene

Rot, Nicolette,De Kanter, Frans J.J.,Bickelhaupt, Friedrich,Smeets, Wilberth J.J.,Spek, Anthony L.

, p. 369 - 379 (2007/10/03)

The reaction of 1,3,5-tribromo- or 1,2,4,5-tetrabromobenzene with trimethylstannyl sodium in tetraglyme gave the corresponding polystannylated benzene derivatives 2 and 4, respectively, in high yield. They were converted with mercuric chloride to the corresponding tris- and tetrakis(chloromercurio)benzenes 5 and 6, respectively. The structure of 5 was confirmed by X-ray crystallography. Some spectral properties of the new compounds are discussed. The (partial) conversion of 2 to 1,3,5-trilithiobenzene (8) was also investigated.

SUBSTITUTED PYRAZOLOPYRIMIDINES AS ANGIOTENSIN II ANTAGONISTS

-

, (2008/06/13)

Novel substituted pyrazolopyrimidines of formula (I) which are useful as angiotensin II antagonists, are disclosed. STR1

SUBSTITUTED IMIDAZOPYRIDAZINES AS ANGIOTENSIN II ANTAGONISTS

-

, (2008/06/13)

Novel substituted imidazopyridazines of formula (I) which are useful as angiotensin II antagonists, are disclosed. STR1

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