Cas 839-34-9,8,9,17,18-Tetraoxadispiro[6.2.6.2]octadecane

839-34-9

Post Buying Request

Basic information

Product Name: 8,9,17,18-Tetraoxadispiro[6.2.6.2]octadecane
Synonyms:
CAS NO:839-34-9
Molecular Formula: C14H24O4
Molecular Weight: 256.342
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: 8,9,17,18-Tetraoxadispiro[6.2.6.2]octadecane(CAS DataBase Reference)
NIST Chemistry Reference: 8,9,17,18-Tetraoxadispiro[6.2.6.2]octadecane(839-34-9)
EPA Substance Registry System: 8,9,17,18-Tetraoxadispiro[6.2.6.2]octadecane(839-34-9)

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: 839-34-9(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

839-34-9 Suppliers

Recommended suppliers

839-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 839-34-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 839-34:
(5*8)+(4*3)+(3*9)+(2*3)+(1*4)=89
89 % 10 = 9
So 839-34-9 is a valid CAS Registry Number.

839-34-9Upstream product

839-34-9Downstream Products

839-34-9Relevant academic research and scientific papers

New preparation of 1,2,4,5-tetraoxanes

Terent'ev,Kutkin,Starikova,Antipin,Ogibin,Nikishin

, p. 2356 - 2366 (2007/10/03)

A convenient procedure was developed for the synthesis of 1,2,4,5-tetraoxanes based on the reaction of gem-bishydroper-oxycycloalkanes with ketals and acetals catalyzed by boron trifluoride etherate, which makes it possible to prepare the target products

Dispiro-1,2,4-trioxolanes by Ozonolysis of Cycloalkylidenecycloalkanes on Polyethylene

Griesbaum, Karl,Krieger-Beck, Petra,Beck, Johannes

, p. 391 - 396 (2007/10/02)

Ozonolyses of symmetrical (1b-d) and of unsymmetrical cycloalkylidenecycloalkanes (8a, b) afforded the dispiro-1,2,4-trioxolanes 4b-d and 9a, b, respectively.Their thermal decompositions gave mixtures of the cyclic ketones (3) and lactones (6).Photolysis afforded in addition to 3 and 6 the cyclic anhydrides 13, which are isomeric with the corresponding disoiro-1,2,4-trioxolanes.

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 839-34-9