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Stannane, tributyl(1-methylenepropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115969-19-2 Structure
  • Basic information

    1. Product Name: Stannane, tributyl(1-methylenepropyl)-
    2. Synonyms:
    3. CAS NO:115969-19-2
    4. Molecular Formula: C16H34Sn
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115969-19-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Stannane, tributyl(1-methylenepropyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Stannane, tributyl(1-methylenepropyl)-(115969-19-2)
    11. EPA Substance Registry System: Stannane, tributyl(1-methylenepropyl)-(115969-19-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 115969-19-2(Hazardous Substances Data)

115969-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115969-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,6 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115969-19:
(8*1)+(7*1)+(6*5)+(5*9)+(4*6)+(3*9)+(2*1)+(1*9)=152
152 % 10 = 2
So 115969-19-2 is a valid CAS Registry Number.

115969-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name but-1-en-2-yl(tributyl)stannane

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:115969-19-2 SDS

115969-19-2Downstream Products

115969-19-2Relevant articles and documents

The Synthesis of Allylstannanes and Vinylstannanes by the Stannyl-cupration of Allenes

Barbero, Asuncion,Cuadrado, Purificacion,Fleming, Ian,Gonzalez, Ana M.,Pulido, Francisco J.

, p. 1030 - 1031 (1990)

Stannyl-cupration of allenes followed by electrophilic attack gives allyl- and vinylstannanes with a variety of substitution patterns; the regiochemistry of the reaction depends upon the temperature and the nature of the stannyl-cuprate reagent.

Synthesis of Allylstannanes and Vinylstannanes by the Stannyl-cupration of Allenes

Barbero, Asuncion,Cuadrado, Purificacion,Fleming, Ian,Gonzalez, Ana M.,Pulido, Francisco J.

, p. 327 - 332 (2007/10/02)

Stannyl-cupration of allenes followed by electrophilic attack gives allyl- and vinyl-stannanes with a variety of substitution patterns.The regiochemistry of the reaction depends upon the temperature at which the intermediate cuprate is quenched with an electrophile.With allene itself, the allylstannane-vinylcuprate 1-(tributylstannylmethyl)vinylcuprate 5, is the product of kinetically controlled addition, but the vinylstannane-allylcuprate 2-(tributylstannyl)allylcuprate 6, is thermodynamically lower in energy.The equilibrium between these isomers begins to take place between -100 and -78 deg C.

THERMAL DECOMPOSITION OF ORGANOTIN SULFAMATES: A ONE POT SYNTHESIS OF VINYLTRIBUTYLTIN COMPOUNDS

Ratier, Max,Khatmi, Djamel,Duboudin, J.Georges,Minh, Dao The

, p. 285 - 292 (2007/10/02)

The preparation of some alkyltributyltin sulfamates is described.Thermal decomposition of these compounds provides a route to vinyltributyltin derivatives.

Synthese et thermolyse eclair d'esters α-tributylstanniques

Duboudin, J. Georges,Ratier, Max,Trouve, Bruno

, p. 181 - 192 (2007/10/02)

The preparation of some alkyltributyltin acetates and thiocarbonates is described.Flash thermolysis of these compounds at high temperature (600-950 deg C) and under a moderate vacuum, provides a new route to vinyltributyltin derivatives.

A NEW ROUTE TO VINYLTRIBUTYLTIN COMPOUNDS BY FLASH PYROLYSIS OF ALKYLTRIBUTYLTIN ACETATES

Duboudin, J. Georges,Petraud, Michel,Ratier, Max,Trouve, Bruno

, p. C6 - C8 (2007/10/02)

Flash pyrolysis of alkyltributyltin acetates, at high temperatures (600-850 deg C) under a moderate vacuum provides a convenient route to vinyltin derivatives.

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