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17887-41-1

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17887-41-1 Usage

General Description

Tert-Butylphenyldichlorosilane, also known as TBPDCS, is a chemical compound belonging to the organosilicon group. It is a clear, colorless liquid with a pungent odor, and is primarily used as a intermediate in the production of other organosilicon compounds. TBPDCS is widely utilized as a key building block in the synthesis of high-performance and specialty silicone products, such as sealants, adhesives, and coatings. Additionally, it is employed as a coupling agent and surface modifier in various industrial applications, including the production of plastics, elastomers, and polymers. TBPDCS is also known for its exceptional reactivity and versatility, making it an important component in the development of advanced materials for various industries. However, it is important to note that TBPDCS should be handled with caution, as it can be corrosive to the skin and eyes and may cause respiratory irritation if inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 17887-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,8 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17887-41:
(7*1)+(6*7)+(5*8)+(4*8)+(3*7)+(2*4)+(1*1)=151
151 % 10 = 1
So 17887-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H14Cl2Si/c1-10(2,3)13(11,12)9-7-5-4-6-8-9/h4-8H,1-3H3

17887-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-dichloro-phenylsilane

1.2 Other means of identification

Product number -
Other names tert-Butyl-dichlor-phenyl-silan

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:17887-41-1 SDS

17887-41-1Relevant articles and documents

Catalytic Enantioselective Dehydrogenative Si-O Coupling to Access Chiroptical Silicon-Stereogenic Siloxanes and Alkoxysilanes

Zhu, Jiefeng,Chen, Shuyou,He, Chuan

supporting information, p. 5301 - 5307 (2021/05/04)

A rhodium-catalyzed enantioselective construction of triorgano-substituted silicon-stereogenic siloxanes and alkoxysilanes is developed. This process undergoes a direct intermolecular dehydrogenative Si-O coupling between dihydrosilanes with silanols or alocohols, giving access to a variety of highly functionalized chiral siloxanes and alkoxysilanes in decent yields with excellent stereocontrol, that significantly expand the chemical space of the silicon-centered chiral molecules. Further utility of this process was illustrated by the construction of CPL-active (circularly polarized luminescence) silicon-stereogenic alkoxysilane small organic molecules. Optically pure bis-alkoxysilane containing two silicon-stereogenic centers and three pyrene groups displayed a remarkable glum value with a high fluorescence quantum efficiency (glum = 0.011, φF = 0.55), which could have great potential application prospects in chiral organic optoelectronic materials.

1-t-Butyl-1-phenyl-1-silacyclohexane: Synthesis, conformational analysis in gas and solution by GED, FT-IR and theoretical calculations

Oznobikhina, Larisa P.,Phien, Tran Dinh,Shainyan, Bagrat A.,Shlykov, Sergey A.,Suslova, Elena N.

, (2020/07/31)

1-t-Butyl-1-phenyl-1-silacyclohexane 1, the first disubstituted silacyclohexane with the most bulky substituent, t-Bu group, at silicon, was synthesized via the sequence of reactions PhSiCl3 → Ph(Cl)Si(CH2)5 → Ph(t-Bu)Si(C

Unpredictable reaction of phenyltrichlorosilane with tert-butyllithium

Scholz, Stefan,S?nger, Inge,Sch?del, Frauke,Bolte, Michael,Lerner, Hans-Wolfram

, p. 50 - 52 (2014/04/17)

The reaction of PhSiCl3 with one equivalent of Li[tBu] at r. t. yielded tBuPhSiCl2 whereas tBu2PhSiCl was only a minor product of the reaction of two molar equivalents Li[tBu] with PhSiCl3 at 60 °C. By contrast,

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