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2954-94-1

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2954-94-1 Usage

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Dicyclohexyltin dibromide is an important chemical compound used in Pharmacology for inhibition of pancreatic cancer cell lines by organotin polyesters.

Check Digit Verification of cas no

The CAS Registry Mumber 2954-94-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2954-94:
(6*2)+(5*9)+(4*5)+(3*4)+(2*9)+(1*4)=111
111 % 10 = 1
So 2954-94-1 is a valid CAS Registry Number.
InChI:InChI=1/2C6H11.2BrH.Sn/c2*1-2-4-6-5-3-1;;;/h2*1H,2-6H2;2*1H;/q;;;;+2/p-2/rC12H22Br2Sn/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2

2954-94-1 Well-known Company Product Price

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  • Alfa Aesar

  • (87800)  Dicyclohexyltin dibromide   

  • 2954-94-1

  • 1g

  • 836.0CNY

  • Detail
  • Alfa Aesar

  • (87800)  Dicyclohexyltin dibromide   

  • 2954-94-1

  • 5g

  • 6933.0CNY

  • Detail

2954-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dibromo(dicyclohexyl)stannane

1.2 Other means of identification

Product number -
Other names Dibromodicyclohexylstannane

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 -
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More Details:2954-94-1 SDS

2954-94-1Relevant articles and documents

A novel route for the preparation of dimeric tetraorganodistannoxanes

Beckmann, Jens,Dakternieks, Dainis,Kuan, Fong Sheen,Tiekink, Edward R.T

, p. 73 - 83 (2007/10/03)

The reaction of polymeric diorganotin oxides, (R2SnO)n (R = Me, Et, n-Bu, n-Oct, c-Hex, i -Pr, Ph), with saturated aqueous NH4X (X = F, Cl, Br, I, OAc) in refluxing 1,4-dioxane afforded in high yields dimeric tetraorganodistannoxanes, [R2(X)SnOSn(X)R2]2, and in a few cases diorganotin dihalides or diacetates, R2SnX2. The reported method appears suitable for the synthesis of fluorinated tetraorganodistannoxanes. Identification of [R2(OH)SnOSn(X)R2]2 (R=n-Bu; X = Cl, Br) and [R2(OH)SnOSn(X)R2] [R2(X)SnOSn(X)R2] suggest a serial substitution mechanism starting from [R2(OH)SnOSn(OH)R2]2. X-ray crystal structure determinations are reported for [Me2(AcO)SnOSn(OAc)Me2]2 (29a), [i-Pr2(Br)SnOSn(Br)i-Pr2]2 (20a), [c-Hex2 (F)SnOSn(F)c-Hex2]2 (5a) and [c-Hex2(F)SnOSn(Cl)c-Hex2]2 (36), respectively. These show the presence of a central (R2Sn)2O2 core that is connected, via the oxygen atoms, to R2Sn entities. Acetate (29a) or halides (5a, 20a, 36) complete the coordination about the tin centres.

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