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5H-Tetrazole-5-thione, 1,4-dihydro-1-phenyl-4-(tributylstannyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30992-56-4

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30992-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30992-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30992-56:
(7*3)+(6*0)+(5*9)+(4*9)+(3*2)+(2*5)+(1*6)=124
124 % 10 = 4
So 30992-56-4 is a valid CAS Registry Number.

30992-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-4-tributylstannyltetrazole-5-thione

1.2 Other means of identification

Product number -
Other names -

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:30992-56-4 SDS

30992-56-4Downstream Products

30992-56-4Relevant academic research and scientific papers

Organotin mediated cycloaddition reactions: a re-investigation of the reaction between organotin azides and isothiocyanates

Deeth, Robert J.,Molloy, Kieran C.,Mahon, Mary F.,Whittaker, Sophie

, p. 25 - 35 (2007/10/02)

Organotin derivatives of 1-organo-5-thiotetrazole (RN4CS) have been synthesized by two methods: (i) a cycloaddition reaction between Bu3SnN3 and RNCS, and (ii) reaction between the sodium salt of the preformed tetrazole and an organotin halide.The structure of Bu2Sn(SCN4Ph)2 has been determined, and the ligand shown to be in the thio form, attached to tin through sulphur, rather than through nitrogen as previously reported.An analysis of the azide-isothiocyanide cycloaddition reaction based upon molecular orbital calculations is presented.

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