Cas 497236-37-0,4-methyl-<i>N</i>-{2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-<i>N</i>-trimethylsilanylethynyl-benzenesulfonamide

497236-37-0

Post Buying Request

Basic information

Product Name: 4-methyl-N-{2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-N-trimethylsilanylethynyl-benzenesulfonamide
Synonyms: 4-methyl-N-{2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-N-trimethylsilanylethynyl-benzenesulfonamide
CAS NO:497236-37-0
Molecular Formula:
Molecular Weight: 481.688
EINECS: N/A
Product Categories: N/A

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: 4-methyl-N-{2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-N-trimethylsilanylethynyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-{2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-N-trimethylsilanylethynyl-benzenesulfonamide(497236-37-0)
EPA Substance Registry System: 4-methyl-N-{2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-N-trimethylsilanylethynyl-benzenesulfonamide(497236-37-0)

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: 497236-37-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

497236-37-0 Suppliers

Recommended suppliers

497236-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497236-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,2,3 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 497236-37:
(8*4)+(7*9)+(6*7)+(5*2)+(4*3)+(3*6)+(2*3)+(1*7)=190
190 % 10 = 0
So 497236-37-0 is a valid CAS Registry Number.

497236-37-0Upstream product

497236-37-0Downstream Products

497236-37-0Relevant academic research and scientific papers

A highly efficient and flexible synthesis of substituted carbazoles by rhodium-catalyzed inter- and intramolecular alkyne cyclotrimerizations

Witulski, Bernhard,Alayrac, Carole

, p. 3281 - 3284 (2007/10/03)

An A→ABC or A→ABCD ring-formation strategy proves extremely efficient for generating substituted carbazoles ([Eq. (1)]; Ts = tosyl). Inter- and intramolecular alkyne cyclotrimerizations mediated by Wilkinson's catalyst provide substituted carbazoles of re

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 497236-37-0