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61214-13-9

methyltris(phenylmethoxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61214-13-9 Structure

  • Basic information

    1. Product Name: methyltris(phenylmethoxy)silane
    2. Synonyms: methyltris(phenylmethoxy)silane
    3. CAS NO:61214-13-9
    4. Molecular Formula: C22H24O3Si
    5. Molecular Weight: 364.50966
    6. EINECS: 262-663-4
    7. Product Categories: N/A
    8. Mol File: 61214-13-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 453°C at 760 mmHg
    3. Flash Point: 233°C
    4. Appearance: /
    5. Density: 1.099g/cm3
    6. Vapor Pressure: 5.73E-08mmHg at 25°C
    7. Refractive Index: 1.565
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: methyltris(phenylmethoxy)silane(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyltris(phenylmethoxy)silane(61214-13-9)
    12. EPA Substance Registry System: methyltris(phenylmethoxy)silane(61214-13-9)

  • 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: 61214-13-9(Hazardous Substances Data)

61214-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61214-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,1 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61214-13:
(7*6)+(6*1)+(5*2)+(4*1)+(3*4)+(2*1)+(1*3)=79
79 % 10 = 9
So 61214-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H24O3Si/c1-26(23-17-20-11-5-2-6-12-20,24-18-21-13-7-3-8-14-21)25-19-22-15-9-4-10-16-22/h2-16H,17-19H2,1H3

61214-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl-tris(phenylmethoxy)silane

1.2 Other means of identification

Product number -
Other names EINECS 262-663-4

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:61214-13-9 SDS

61214-13-9Relevant articles and documents

Silanol Compound, Composition, and Method for Producing Silanol Compound

-

Paragraph 0158, (2017/07/14)

The purpose of the present invention is to provide silanol compounds that can be used as raw materials of siloxane compounds and the like, and a composition of the silanol compounds, as well as to provide a production method that makes it possible to produce silanol compounds at excellent yield. A composition comprising 5 mass % to 100 mass % of a silanol compound represented by Formulas (A) to (C) can be prepared by devising to produce silanol compounds under water-free conditions, to produce silanol compounds in a solvent having the effect of suppressing the condensation of silanol compounds, and to perform other such processes, the composition being able to be used as a raw material or the like of siloxane compounds because the silanol compounds can be stably present in the resulting composition.

Chiral Acylsilanes in Organic Synthesis. Diastereoselective 1,2 Additions to Racemic Alkoxymethyl-Substituted Acylsilanes

Bienz, Stefan,Chapeaurouge, Alexander

, p. 1477 - 1488 (2007/10/02)

The synthesis of the three alkoxymethyl-sustituted acylsilanes 1-3 is described (Schemes 1 and 2).Their reactions with NaBH4 as well as PhLi gave the corresponding alcohols with moderate to good diastereoisomeric induction (up to 78percent de; see Table), depending upon the solvent used (Scheme 3).The results indicate that in Et2O, the reactions with PhLi proceed via 6-membered chelates (see C in Scheme 4) leading to the products with high de's (74 - 78percent).In THF, these chelates are not formed, and as a consequence, the additions take place with reversed and lower stereoselectivities (34 - 50percent de).

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