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Silane, [2,6-bis(1,1-dimethylethyl)-4-methylphenoxy]chlorodimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90101-29-4

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90101-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90101-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90101-29:
(7*9)+(6*0)+(5*1)+(4*0)+(3*1)+(2*2)+(1*9)=84
84 % 10 = 4
So 90101-29-4 is a valid CAS Registry Number.

90101-29-4SDS

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 chloro-(2,6-ditert-butyl-4-methylphenoxy)-dimethylsilane

1.2 Other means of identification

Product number -
Other names 2,6-Di-t-butyl-4-methylphenoxydimethylchlorosilane

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:90101-29-4 SDS

90101-29-4Relevant academic research and scientific papers

Sterically crowded aryloxide compounds of silicon

Healy, Matthew D.,Barron, Andrew R.

, p. 165 - 172 (2007/10/02)

The interaction of one equivalent of NaBHT (BHT-H = butylated hydroxytoluene) with Me3SiCl, Me2SiCl2 and SiCl4 gives Me3Si(BHT) (1), Me2SiCl(BHT) (2) and Cl3Si(BHT) (3), respectively, which have been characterized by 1H NMR, IR spectroscopy and elemental

Symmetrical Alkoxysilyl Ethers. A New Class of Alcohol-Protecting Groups. Preparation of tert-Butoxydiphenylsilyl Ethers

Gillard, John W.,Fortin, Rejean,Morton, Howard E.,Yoakim, Christiane,Quesnelle, Claude A.,at al.

, p. 2602 - 2608 (2007/10/02)

The preparation and evaluation of a new class of alcohol-protecting groups, the alkoxydiphenylsilyl ethers, are described.In particular, tert-butoxydiphenylsilyl ethers, which can be formed from primary, secondary, or tertiary alcohols and tert-butoxydiphenylsilyl chloride, offer the useful synthetic properties of acid stability and high fluoride reactivity.Opportunities for selective silyl group cleavage are highlighted.

Silyl isothiocyanates

-

, (2008/06/13)

The invention concerns novel compounds of formula IIIA wherein Ra is selected from electron donating substituents consisting of alkoxy of 1-10 carbon atoms, cycloalkoxy of 4-8 carbon atoms, aralkoxy of 7-12 carbon atoms, phenoxy which may b

5,6,7,8-Tetrahydroquinolines. Part 6. Silylation vs. Thioamidation in the Reaction of Silyl Isothiocyanates with Organometallics: Influence of the Solvent and of the Substituent on Silicon.

Crossley, Roger,Shepherd, Robin G.

, p. 1917 - 1920 (2007/10/02)

The influence of a number of variables on carbophilic vs. silicophilic attack by 8-lithio-3-methyl-5,6,7,8-tetrahydroquinoline on silyl isothiocyanates is reported.In general carbophilic attack (i.e. thiomidation) is favoured in solvents of low polarity a

Preparation of fused carbocyclic ring derivatives of pyridine

-

, (2008/06/13)

An improved process for preparing fused carbocyclic ring derivatives of pyridine especially 5,6,7,8-tetrahydroquinoline 8-nitriles, amides and thioamides is described. The nitriles and thioamides are anti-ulcer and/or anti-secretory agents. Typically a co

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