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1873-89-8

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1873-89-8 Usage

Chemical Properties

Clear colorless liquid

Application

Gives highly stereoselective reduction of substituted cyclohexanones.

Check Digit Verification of cas no

The CAS Registry Mumber 1873-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1873-89:
(6*1)+(5*8)+(4*7)+(3*3)+(2*8)+(1*9)=108
108 % 10 = 8
So 1873-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H27O3Si4/c1-14(2,3)10-13(11-15(4,5)6)12-16(7,8)9/h1-9H3

1873-89-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L16686)  Tris(trimethylsiloxy)silane, 97%   

  • 1873-89-8

  • 5g

  • 235.0CNY

  • Detail
  • Alfa Aesar

  • (L16686)  Tris(trimethylsiloxy)silane, 97%   

  • 1873-89-8

  • 25g

  • 1001.0CNY

  • Detail
  • Aldrich

  • (370908)  Tris(trimethylsiloxy)silane  ≥98%

  • 1873-89-8

  • 370908-25G

  • 1,083.42CNY

  • Detail

1873-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(trimethylsilyloxy)silicon

1.2 Other means of identification

Product number -
Other names Tris(trimethylsiloxy)silane

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:1873-89-8 SDS

1873-89-8Downstream Products

1873-89-8Relevant articles and documents

1,1,1,5,5,5-HEXAMETHYLTRISILOXANE: PREPARATION AND SOME REACTIONS

Seyferth, Dietmar,Prud'homme, Christian C.,Wang, Wei-Liang

, p. 203 - 210 (1984)

1,1,1,5,5,5-Hexamethyltrisiloxane (I) was prepared by reaction of (Me3SiO)2Mg or of Me3SiOH with dichlorosilane.Its selective chlorination to give mostly Me3SiOSiHClOSiMe3 and only a small amount of Me3SiOSiCl2OSiMe3 was effected by its PdCl2-catalyzed reaction with CCl4.Photolysis of compound I gave H(Me3SiO)2SiSi(OSiMe3)2H in 30percent yield, as well as polymer.

Aerobic Co or Cu/NHPI-catalyzed oxidation of hydride siloxanes: Synthesis of siloxanols

Arzumanyan, Ashot V.,Goncharova, Irina K.,Novikov, Roman A.,Milenin, Sergey A.,Boldyrev, Konstantin L.,Solyev, Pavel N.,Tkachev, Yaroslav V.,Volodin, Alexander D.,Smol'Yakov, Alexander F.,Korlyukov, Alexander A.,Muzafarov, Aziz M.

supporting information, p. 1467 - 1471 (2018/04/12)

A highly efficient preparative method for the synthesis of siloxanols based on aerobic Co(OAc)2 or Cu(OAc)2/NHPI-catalyzed oxidation of hydride siloxanes using "green", commercially available, simple inexpensive reagents and mild reaction conditions has been proposed. This is a general reaction for the synthesis of mono-, oligo- and polymeric siloxanols with various structures (linear, branched and cyclic).

Untersuchungen zu Substituenteneffekten in Tris(methylorganophenylsiloxy)silanen (RMePhSiO)3SiH

Popowski, Eckhard,Kraft, Oliver,Kelling, Hans,Jancke, Harald

, p. 30 - 31 (2007/10/02)

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