Cas 113793-64-9,Silane, [[1-(2,2-dimethyl-6-methylenecyclohexylidene)-2-propenyl]oxy]trimethyl-, (Z)-

113793-64-9

Post Buying Request

Basic information

Product Name: Silane, [[1-(2,2-dimethyl-6-methylenecyclohexylidene)-2-propenyl]oxy]trimethyl-, (Z)-
Synonyms:
CAS NO:113793-64-9
Molecular Formula: C15H26OSi
Molecular Weight: 250.456
EINECS: N/A
Product Categories: N/A
Mol File: 113793-64-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Silane, [[1-(2,2-dimethyl-6-methylenecyclohexylidene)-2-propenyl]oxy]trimethyl-, (Z)-(CAS DataBase Reference)
NIST Chemistry Reference: Silane, [[1-(2,2-dimethyl-6-methylenecyclohexylidene)-2-propenyl]oxy]trimethyl-, (Z)-(113793-64-9)
EPA Substance Registry System: Silane, [[1-(2,2-dimethyl-6-methylenecyclohexylidene)-2-propenyl]oxy]trimethyl-, (Z)-(113793-64-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 113793-64-9(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

113793-64-9 Suppliers

Recommended suppliers

113793-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113793-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,9 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113793-64:
(8*1)+(7*1)+(6*3)+(5*7)+(4*9)+(3*3)+(2*6)+(1*4)=129
129 % 10 = 9
So 113793-64-9 is a valid CAS Registry Number.

113793-64-9Upstream product

113793-64-9Downstream Products

113793-64-9Relevant academic research and scientific papers

Reaction of Ester Enolates with Nucleophiles. Stereocontrolled Formation of Ketone and Aldehyde Enolates

Fehr, Charles,Galindo, Jose

, p. 1828 - 1830 (2007/10/02)

Lithium enolates of carboxylic and thiocarboxylic esters react with nucleophiles to afford ketone and aldehyde enolates and subsequently their enol silyl ethers diastereoselectively.This reaction is applied to the synthesis of γ-damascone, α-damascone, β-safranal, and artemisia ketone.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

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)

What can I do for you?
Get Best Price

Get Best Price for 113793-64-9