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N,N-dimethyl-3-(tributylstannanyl)propan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29346-31-4

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29346-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29346-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,4 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29346-31:
(7*2)+(6*9)+(5*3)+(4*4)+(3*6)+(2*3)+(1*1)=124
124 % 10 = 4
So 29346-31-4 is a valid CAS Registry Number.

29346-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-3-tributylstannylpropan-1-amine

1.2 Other means of identification

Product number -
Other names Propylamine,N,N-dimethyl-3-(tributylstannyl)-(8CI)

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:29346-31-4 SDS

29346-31-4Downstream Products

29346-31-4Relevant academic research and scientific papers

DIRECTED CLEAVAGE OF CARBON-TIN BONDS BY PALLADIUM

Suggs, J. William,Lee, Ken. S.

, p. 297 - 310 (2007/10/02)

The ligands 8-(trimethylstannyl)methylquinoline, n-Bu3Sn(CH2)3NMe2 and Ph3Sn(CH2)3NMe2 Ph3Sn(CH2)3NMe2 react with (C6H5CN)2PdCl2 to give five-membered palladium chelates, in which the nitrogen atom was able to direct palladium insertion into a specific carbon-tin bond.The X-ray crystal structure of the simple chelate 2 is presented.

Antifungal and/or antibacterial organotin compounds, and use

-

, (2008/06/13)

Antifungal and/or antibacterial organotin compounds characterized by the formula in which R1, R2 and R3 represent linear or branched alkyl groups having at most 5 carbon atoms or aryl groups, X represents a functional group linked to a carbon atom, x, y, z, n, p and q are integers, n being 1 to 4 inclusive, p being 1 to 3 inclusive, q being 1 or 2, and if q=2 then x+y+Z=2 and p=1 and if q=1 then x+y+z=3, and methods for preparing said compounds, and methods for using said compounds for controlling fungi and/or bacteria.

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