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16722-09-1

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16722-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16722-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16722-09:
(7*1)+(6*6)+(5*7)+(4*2)+(3*2)+(2*0)+(1*9)=101
101 % 10 = 1
So 16722-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H12OSi/c1-7(2,3)5-4-6-5/h5H,4H2,1-3H3

16722-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(oxiran-2-yl)silane

1.2 Other means of identification

Product number -
Other names 1,2-epoxyethyltrimethylsilane

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:16722-09-1 SDS

16722-09-1Upstream product

16722-09-1Relevant articles and documents

Kinetics of Iron(III) Porphyrin Catalyzed Epoxidations

Traylor, Teddy G.,Marsters, James C.,Nakano, Taku,Dunlap, Beth E.

, p. 5537 - 5539 (1985)

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Method for synthesizing 2-phenyl-2-trimethylsilyl acetyl chloride from trimethyl (vinyl) silane

-

Paragraph 0008-0010, (2018/05/01)

The invention relates to a method for synthesizing 2-phenyl-2-trimethylsilyl acetyl chloride from trimethyl (vinyl) silane, to mainly solve the technical problem that an industrial synthesis method ofthe compound is in shortage. The method comprises the following three steps: step 1, dissolving trimethyl(vinyl)silane in dichloromethane, and adding 3-chloroperoxybenzoic acid at a low temperature for reaction to obtain trimethyl (2-epoxyethyl)silane; step 2, dissolving phenyl magnesium bromide and cuprous cyanide in isopropyl ether at a low temperature, and adding trimethyl(2-epoxyethyl)silanefor reaction to generate 2-phenyl-2-trimethylsilyl ethanol; step 3, carrying out a reaction of a tetrahydrofuran solution of the 2-phenyl-2-trimethylsilyl ethanol under the condition with triethylamine and triphosgene to generate 2-phenyl-2-trimethylsilyl acetyl chloride.

The (2-Phenyl-2-trimethylsilyl)ethyl-(PTMSEL)-Linker in the Synthesis of Glycopeptide Partial Structures of Complex Cell Surface Glycoproteins

Wagner, Michael,Dziadek, Sebastian,Kunz, Horst

, p. 6018 - 6030 (2007/10/03)

The (2-phenyl-2-trimethylsilyl)ethyl-(PTMSEL) linker represents a novel fluoride-sensitive anchor for the solid-phase synthesis of protected peptides and glycopeptides. Its cleavage is achieved under almost neutral conditions using tetrabutylammonium fluo

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