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1199-95-7

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1199-95-7 Usage

Chemical Properties

white to light beige crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 1199-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1199-95:
(6*1)+(5*1)+(4*9)+(3*9)+(2*9)+(1*5)=97
97 % 10 = 7
So 1199-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5.3CH3.Sn/c1-2-8-6-4-3-5-7-8;;;;/h3-7H;3*1H3;/rC11H14Sn/c1-12(2,3)10-9-11-7-5-4-6-8-11/h4-8H,1-3H3

1199-95-7 Well-known Company Product Price

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  • Aldrich

  • (429953)  Trimethyl(phenylethynyl)tin  97%

  • 1199-95-7

  • 429953-1G

  • 998.01CNY

  • Detail

1199-95-7SDS

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 trimethyl(2-phenylethynyl)stannane

1.2 Other means of identification

Product number -
Other names Stannane,trimethyl(2-phenylethynyl)

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:1199-95-7 SDS

1199-95-7Relevant articles and documents

Lappert, M. F.,Lorberth, J.,Poland, J. S.

, (1970)

Fluoride ion mediated reactions of disubstituted acetylenes Me3SiCCMMe3 (M=C, Si, Ge, Sn) with terminal acetylenes

Lukevics, Edmunds,Rubina, Kira,Abele, Edgars,Fleisher, Mendel,Arsenyan, Pavel,Grinberga, Solveiga,Popelis, Juris

, p. 69 - 73 (2007/10/03)

The CsF-18-crown-6 mediated reactions of disubstituted acetylenes Me3SiCCMMe3 (M=C, Si, Ge, Sn) with phenylacetylene and 2-methyl-5-pyridylacetylene in benzene have been studied. The first step of the reaction is the deprotonation of

Alkynyl-siibstituted tricarbonyl(cyclobutadlene)iron complexes: coupling of complexes sfannylalkynes

Bunz, Uwe H. F.,Jutta

, p. 785 - 797 (2007/10/03)

The synthesis of mono-, di-, tri- and tetraalkynylated tricartaonyl(cyclobutadiene)iron complexes is accomplished by a repetitive metalation/iodination/coupling sequence. Application of this sequence leads to the synthesis of oligomeric cyclobutadiene complexes with various topologies, inter alia to the synthesis of a perethynylated aimer 24. Alternatively a one-step coupling procedure (Stille-Farina) has been used to synthesize tetraalkynylated tricarbonyl(cyclobutadiene)irons 26, VCH Verlagsgesellschaft mbH, : 1996.

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