Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2767-54-6

Post Buying Request

2767-54-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2767-54-6 Usage

Chemical Properties

colourless liquid

General Description

Clear colorless liquid.

Air & Water Reactions

TRIETHYLTIN BROMIDE is sensitive to moisture. Slightly water soluble.

Reactivity Profile

TRIETHYLTIN BROMIDE is incompatible with strong oxidizers. Corrosive. .

Hazard

Moderately toxic by inhalation. A repro- ductive hazard.

Fire Hazard

TRIETHYLTIN BROMIDE is combustible.

Safety Profile

Moderately toxic by inhalation. Experimental reproductive effects. See also TIN COMPOUNDS and BROMIDES. When heated to decomposition it emits toxic fumes of Br-.

Check Digit Verification of cas no

The CAS Registry Mumber 2767-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2767-54:
(6*2)+(5*7)+(4*6)+(3*7)+(2*5)+(1*4)=106
106 % 10 = 6
So 2767-54-6 is a valid CAS Registry Number.
InChI:InChI=1/3C2H5.BrH.Sn/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1/rC6H15BrSn/c1-4-8(7,5-2)6-3/h4-6H2,1-3H3

2767-54-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (71135)  Triethyltin bromide   

  • 2767-54-6

  • 1g

  • 344.0CNY

  • Detail
  • Alfa Aesar

  • (71135)  Triethyltin bromide   

  • 2767-54-6

  • 5g

  • 1066.0CNY

  • Detail
  • Alfa Aesar

  • (71135)  Triethyltin bromide   

  • 2767-54-6

  • 25g

  • 5691.0CNY

  • Detail
  • Aldrich

  • (288047)  Triethyltinbromide  97%

  • 2767-54-6

  • 288047-1G

  • 475.02CNY

  • Detail
  • Aldrich

  • (288047)  Triethyltinbromide  97%

  • 2767-54-6

  • 288047-5G

  • 1,471.86CNY

  • Detail

2767-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bromo(triethyl)stannane

1.2 Other means of identification

Product number -
Other names Bromotriethylstannane

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:2767-54-6 SDS

2767-54-6Relevant articles and documents

Chernoplekova et al.

, (1975)

Spin chemistry of organometallic compounds: Part 1. Interaction of N-bromohexamethyldisilazane with allyltriethylstannane

Taraban, Marc B.,Kruppa, Alexander I.,Rakhlin, Vladimir I.,Grigor'Ev, Stanislav I.,Volkova, Olga S.,Mirskov, Rudolph G.,Leshina, Tatyana V.

, p. 12 - 16 (2001)

It has been shown, on the basis of the analysis of CIDNP effects, that allene and (Me3Si)2NH - major products of the photoinduced reaction of Et3SnCH2CH=CH2 and (Me3Si)2NBr - result from a radical pair comprised of ·CH2CHBrCH2SnEt3 and ·N(SiMe3)2 free radicals. Allene is formed through the β-cleavage of the short-lived homolytic substitution product Et3SnCH2CBr=CH2.

AN INVESTIGATION OF THE MECHANISM OF THE REACTION OF ALLYLTRIETHYLSTANNANE WITH BROMOTRICHLOROMETHANE BY RADIOFREQUENCY PROBING AND CHEMICALLY INDUCED DYNAMIC NUCLEAR POLARIZATION (CIDNP)

Leshina, T.V.,Sagdeev, R.Z.,Polyakov, N.E.,Taraban, M.B.,Valyaev, V.I.,et al.

, p. 295 - 300 (1983)

The methods of radiofrequency probing (RFP) and chemcally induced dynamic nuclear polarization (CIDNP) have been used to study the mechanism of the reaction of allyltriethylstannane with bromotrichloromethane.The CIDNP effects which have been detected prove the presence of radical stages in this reaction.An assumption has been made about a possible radical pathway for the β-decomposition of elementorganic compounds.

Homolytic addition of polyhaloalkanes to α-vinyloxy-ω-trialkylstannoxyalkanes as a new route to 2-perhaloalkylmethyl-substituted 1,3-dioxacyclanes

Arbuzov, P. V.,Voronkov, M. G.,Mirskov, R. G.,Stankevich, V. K.,Kukharev, B. F.,et al.

, p. 1755 - 1757 (2007/10/03)

Photoinduced reactions of α-vinyloxy-ω-trialkylstannoxyalkanes, CH2=CHO(CH2)nOSnEt3 (n = 2 to 4), with polyhaloalkanes results in 2-perhaloalkylmethyl-substituted 1,3-dioxacyclanes. - Key words: α-vinyloxy-ω-trialkylstannoxyalkanes, polyhaloalkanes, photoinduced reactions; 1,3-dioxacyclanes.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2767-54-6