14629-62-0

• 

• Basic information

  1. Product Name: Phenethyl(triethylsilyl) ether
  2. Synonyms: (Triethylsilyl)phenethyl ether;Phenethyl(triethylsilyl) ether;Phenethyloxytriethylsilane;Triethylphenethyloxysilane
  3. CAS NO:14629-62-0
  4. Molecular Formula: C₁₄H₂₄OSi
  5. Molecular Weight: 236.43
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 14629-62-0.mol
  9. Article Data: 24

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 279.5±19.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 0.897±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Phenethyl(triethylsilyl) ether(CAS DataBase Reference)
  10. NIST Chemistry Reference: Phenethyl(triethylsilyl) ether(14629-62-0)
  11. EPA Substance Registry System: Phenethyl(triethylsilyl) ether(14629-62-0)

• 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: 14629-62-0(Hazardous Substances Data)

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• SDS
• Upstream product
• Downstream Products
• Article

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14629-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14629-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14629-62:
(7*1)+(6*4)+(5*6)+(4*2)+(3*9)+(2*6)+(1*2)=110
110 % 10 = 0
So 14629-62-0 is a valid CAS Registry Number.

14629-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	triethyl(2-phenylethoxy)silane

1.2 Other means of identification

Product number	-
Other names	Et3SiOCH2CH2Ph

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:14629-62-0 SDS

14629-62-0Upstream product

• 60-12-8 2-phenylethanol 
• 89597-33-1 (E)-1-methoxy-1-(triethylsiloxy)propene 
• 617-86-7 triethylsilane 
• 122-78-1 phenylacetaldehyde 
• 101-97-3 Ethyl 2-phenylethanoate 
• 3558-60-9 1-methoxy-2-phenylethane 
• 18406-24-1 1-(triethylsilyloxy)-4-methoxybenzene 
• 18296-01-0 triethylsilyl formate 
• 4249-72-3 2-phenoxy-1-phenylethanol 
• 96-09-3 styrene oxide 
• 994-30-9 triethylsilyl chloride 
• 1112-54-5 vinyltriethylsilane 
• 55453-17-3 triethyl((1-methoxy-2-methylprop-1-en-1-yl)oxy)silane 

14629-62-0Downstream Products

• 103-45-7 acetic acid phenethyl ester 
• 60-12-8 2-phenylethanol 
• 100-41-4 ethylbenzene 
• 1861-04-7 2-deuterioethylbenzene 

14629-62-0Relevant articles and documents

Mechanism of the dehydrogenative silylation of alcohols catalyzed by cationic gold complexes: An experimental and theoretical study

Labouille, Stephanie,Escalle-Lewis, Aurelie,Jean, Yves,Mezailles, Nicolas,Leafloch, Pascal

, p. 2256 - 2265 (2011)

The catalytic activity both of cationic [(XDPP)Au][X] (XDPP=bis-2,5- diphenylphosphole xantphos X=BF4) and of the isolated gold hydride complex [(XDPP)2Au2H][OTf] in the dehydrogenative silylation process is presented. A p

Use of Silylated Formiates as Hydrosilane Equivalents

-

Paragraph 0514, (2021/09/26)

The present invention relates to a method for preparing organic compounds of formula (I) by reaction between a silylated formiate of formula (II) and an organic compound in the presence of a catalyst and optionally of an additive. The invention also relates to use of the method for preparing organic compounds of formula (I) for the preparation of reagents for fine chemistry and for heavy chemistry, as well as in the production of vitamins, pharmaceutical products, adhesives, acrylic fibres, synthetic leathers, and pesticides.

Hydrosilylation of Carbonyls Catalyzed by Hydridoborenium Borate Salts: Lewis Acid Activation and Anion Mediated Pathways

Rawat, Sandeep,Bhandari, Mamta,Porwal, Vishal Kumar,Singh, Sanjay

supporting information, p. 7195 - 7203 (2020/05/18)

The electronically unsaturated three-coordinated hydridoborenium cations [LBH]+[HB(C6F5)3]-(1) and [LBH]+[B(C6F5)4]-(2), supported by a bis(phosphinimino)amide ligand, were found to be excellent catalysts for hydrosilylation of a range of aliphatic and ar

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