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Benzenamine, 2-[(trimethylsilyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36309-44-1 Structure
  • Basic information

    1. Product Name: Benzenamine, 2-[(trimethylsilyl)oxy]-
    2. Synonyms:
    3. CAS NO:36309-44-1
    4. Molecular Formula: C9H15NOSi
    5. Molecular Weight: 181.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36309-44-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzenamine, 2-[(trimethylsilyl)oxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, 2-[(trimethylsilyl)oxy]-(36309-44-1)
    11. EPA Substance Registry System: Benzenamine, 2-[(trimethylsilyl)oxy]-(36309-44-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 36309-44-1(Hazardous Substances Data)

36309-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36309-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36309-44:
(7*3)+(6*6)+(5*3)+(4*0)+(3*9)+(2*4)+(1*4)=111
111 % 10 = 1
So 36309-44-1 is a valid CAS Registry Number.

36309-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name O-trimethylsilyl-2-aminophenol

1.2 Other means of identification

Product number -
Other names 2-trimethylsilyloxyaniline

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:36309-44-1 SDS

36309-44-1Relevant articles and documents

Bonding interactions in uranyl α-diimine complexes: A spectroscopic and electrochemical study of the impacts of ligand electronics and extended conjugation

Niklas, Julie E.,Hunter, Katherine M.,Gorden, Anne E. V.

, p. 15088 - 15100 (2019)

Uranyl complexes of aryl-substituted α-diimine ligands gbha (UO2-1a-f) and phen-BIAN (UO2-2a-f) [gbha (1) = glyoxal bis(2-hydroxyanil); phen-BIAN (2) = N,N′-bis(iminophenol)acenaphthene; R = OMe (a), t-bu (b), H (c), Me (d), F (e), a

Reaction of 1,5-dimethyl-2,3,3,4-tetrachloro-1,5,2,4-diazadiphosphorinan-6- one with aniline derivatives, heptamethyldisilazane and tert.-butylamine: Oxidative addition of tetrachloro-o-benzoquinone to some P(III)-containing products

Krill, Jochen,Shevchenko, Igor V.,Fischer, Axel,Jones, Peter G.,Schmutzler, Reinhard

, p. 1217 - 1239 (2006)

The reaction of the title compound 1 with the p-R-aniline derivatives (R=H, F, OCH3, NO2, and NH2) led to the formation of the aza-2σ3, 4σ3-diphosphetidines 2a-2e, whereas 2-trimethylsiloxyaniline fur

Synthesis and structural features of N-[(2-(trimethylsilyl)oxy)phenyl]-arylsulfonamides

Nikonov, Alexey Yu,Sterkhova, Irina V.,Serykh, Valeriy Yu,Kolyvanov, Nikita A.,Lazareva, Natalya F.

, (2019)

N-[(2-(Trimethylsilyl)oxy)phenyl]-4-methylbenzenesulfonamide and N-[(2-trimethylsilyloxy)phenyl]-4-chlorobenzenesulfonamide were prepared by two different methods. Their structures were studied by X-ray single-crystal analysis and DFT calculations includi

Synthesis and characterization of a bifunctional nanomagnetic solid acid catalyst (Fe3O4@CeO2/SO42?) and investigation of its efficiency in the protection process of alcohols and phenols via hexamethyldisilazane under solvent-free conditions

Mohammadiyan, Esmaeel,Ghafuri, Hossein,Kakanejadifard, Ali

, p. 171 - 178 (2018/09/12)

In this research, Fe3O4@CeO2 (FC) was synthesized using the coprecipitation method and functionalized by an ammonium sulfate solution to achieve a heterogeneous solid acid Fe3O4@CeO2/SO42? (FCA) catalyst. The synthesized bifunctional catalyst was used in the protection process of alcohols and phenols using hexamethyldisilazane (HMDS) at ambient temperature under solvent-free conditions. Due to its excellent magnetic properties, FCA can easily be separated from the reaction mixture and reused several times without significant loss in its catalytic activity. Excellent yield and selectivity, simple separation, low cost, and high recyclability of the nanocatalyst are outstanding advantages of this procedure. The characterization was carried out using different techniques such as Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and vibrating sample magnetometry (VSM).

Pos [...] 4 group metal olefin polymerization catalyst

-

Paragraph 0506-0508, (2019/08/27)

Embodiments are directed to phosphaguanidine metal complexes of formula I and using those complexes in α-olefin polymerization systems.

Nano Fe3O4@ZrO2/SO42?: A highly efficient catalyst for the protection and deprotection of hydroxyl groups using HMDS under solvent-free condition

Ghafuri, Hossein,Paravand, Fatemeh,Rashidizadeh, Afsaneh

supporting information, p. 129 - 135 (2016/12/24)

In this work, we introduce a new procedure for the protection and deprotection process of various types of alcohols and phenols by HMDS in the presence of nano magnetic sulfated zirconia (Fe3O4@ZrO2/SO42?) as a solid acid catalyst under very mild and solvent-free condition. This method has interesting advantages like short reaction times and a simple workup process. With regard to some outstanding benefits of this new heterogeneous catalyst such as excellent yield, reusability of the catalyst and easy thermal stability, high acidity, strong and excellent magnetic properties, this method can be very interesting in aspect of green chemistry Principles.

Chlorozincate(II) acidic ionic liquid: Efficient and biodegradable silylation catalyst

Abbasi, Faezeh,Azizi, Najmedin,Abdoli-Senejani, Masumeh

, (2017/09/30)

A practical and highly efficient silylation of alcohol and phenol derivatives with hexamethyldisilazane (HMDS) using acidic ionic liquids under mild reaction conditions is described. A series of Br?nsted as well as Br?nsted–Lewis acidic ionic liquids were prepared and their performance investigated for the silylation of a wide variety of alcohols and phenols with HMDS. Imidazole- as well as N-methyl-2-pyrrolidone-based acidic ionic liquids have a higher catalytic activity for the protection of sensitive, hindered alcohols and phenols, thus providing an environmentally begin and versatile alternative to current acid catalysts. In addition, the acidic ionic liquids are reusable, being recovered easily and reused several times without significant deterioration in catalytic activity.

Preparation and characterization of a RHA/TiO2 nanocomposite: Introduction of an efficient and reusable catalyst for chemoselective trimethylsilyl protection and deprotection of alcohols and phenols

Seddighi, Mohadeseh,Shirini, Farhad,Goli-Jolodar, Omid

, p. 23564 - 23570 (2016/03/12)

In this work, rice husk ash (RHA), as a natural source of amorphous silica, was used as a support for the synthesis of anatase-phase titania nanoparticles leading to the RHA/TiO2 nanocomposite. This nanocomposite was used as an efficient catalyst for the chemoselective trimethylsilylation of various alcohols and phenols and deprotection of the obtained trimethylsilyl ethers. The procedure gave the products in excellent yields in very short reaction times. Also this catalyst can be reused at least six times without loss of its catalytic activity.

Nanomagnetic zirconia-based sulfonic acid (Fe3O4@ZrO2-Pr-SO3H): A new, efficient and recyclable solid acid catalyst for the protection of alcohols: Via HMDS under solvent free conditions

Tadjarodi, Azadeh,Khodikar, Rahim,Ghafuri, Hosssein

, p. 63480 - 63487 (2016/07/19)

In the present work, sulfonic acid functionalized nanomagnetic zirconia is prepared by the reaction of (3-mercaptopropyl)trimethoxysilane and nanomagnetic zirconia. Then, nanomagnetic zirconia-based sulfonic acid (Fe3O4@ZrO2/su

RuIII(OTf)SalophenCH2-NHSiO2-Fe: An efficient and magnetically recoverable catalyst for trimethylsilylation of alcohols and phenols with hexamethyldisilazane

Torki, Maryam,Tangestaninejad, Shahram,Mirkhani, Valiollah,Moghadam, Majid,Mohammadpoor-Baltork, Iraj

, p. 304 - 309 (2014/04/03)

Efficient trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) catalyzed by ruthenium(III) complex of chloromethylated Salophen supported on nanomagnetic materials is reported. First, the iron nanomagnets were silica coated, functi

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