Welcome to LookChem.com Sign In|Join Free

CAS

  • or

18306-29-1

Post Buying Request

18306-29-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

18306-29-1 Usage

Chemical Properties

beige to brownish low melting crystals and/or

Check Digit Verification of cas no

The CAS Registry Mumber 18306-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,0 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18306-29:
(7*1)+(6*8)+(5*3)+(4*0)+(3*6)+(2*2)+(1*9)=101
101 % 10 = 1
So 18306-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H18O4SSi2/c1-12(2,3)9-11(7,8)10-13(4,5)6/h1-6H3

18306-29-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (B1245)  Bis(trimethylsilyl) Sulfate  >98.0%(T)

  • 18306-29-1

  • 5g

  • 320.00CNY

  • Detail
  • TCI America

  • (B1245)  Bis(trimethylsilyl) Sulfate  >98.0%(T)

  • 18306-29-1

  • 25g

  • 790.00CNY

  • Detail
  • Alfa Aesar

  • (B23608)  Bis(trimethylsilyl) sulfate, 97%   

  • 18306-29-1

  • 5g

  • 417.0CNY

  • Detail
  • Alfa Aesar

  • (B23608)  Bis(trimethylsilyl) sulfate, 97%   

  • 18306-29-1

  • 25g

  • 849.0CNY

  • Detail
  • Alfa Aesar

  • (B23608)  Bis(trimethylsilyl) sulfate, 97%   

  • 18306-29-1

  • 100g

  • 2690.0CNY

  • Detail

18306-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(trimethylsilyl) sulfate

1.2 Other means of identification

Product number -
Other names Bistrimethylsilylsulfate

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:18306-29-1 SDS

18306-29-1Relevant articles and documents

Appel,Frechen

, p. 125,127 (1977)

Catalytic Disproportionation of Formic Acid to Methanol by using Recyclable Silylformates

Cantat, Thibault,Chauvier, Clément,Imberdis, Arnaud,Thuéry, Pierre

supporting information, p. 14019 - 14023 (2020/06/09)

A novel strategy to prepare methanol from formic acid without an external reductant is presented. The overall process described herein consists of the disproportionation of silyl formates to methoxysilanes, catalyzed by ruthenium complexes, and the production of methanol by simple hydrolysis. Aqueous solutions of MeOH (>1 mL, >70 percent yield) were prepared in this manner. The sustainability of the reaction has been established by recycling of the silicon-containing by-products with inexpensive, readily available, and environmentally benign reagents.

The efficient method for the preparation of alkenylsilanes from organoaluminums

Kadikova, Rita N.,Zosim, Tat'Yana P.,Dzhemilev, Usein M.,Ramazanov, Ilfir R.

, p. 14 - 19 (2014/05/20)

Silyl esters of sulfonic acids are convenient and efficient silylating agents for β,β- and β-substituted 1-alkenylaluminums. The reaction proceeds at room temperature in CH2Cl2 or hexane for 18 h to give corresponding alkenylsilanes in high yield. At the same time, α,β-disubstituted and α,β,β-trisubstituted 1-alkenylaluminums were inert in the reaction under study. The reaction with aluminacyclopen-2-enes and aluminacyclopentanes takes place on the less sterically hindered reaction center. Using electron-donating solvents (diethyl ether, THF) inhibits the reaction. A new convenient procedure of silylation was developed, which consists in obtaining the silyl tosylate by the reaction of chlorosilanes with anhydrous sodium tosylate in toluene solution. The resulting reaction mixture was reacted with organoaluminum compounds without isolation of silyl tosylate.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 18306-29-1