Cas 186258-72-0,(2R,4S,5R)-5-Allyloxy-2-(4-methoxy-phenyl)-4-pent-4-enyl-[1,3]dioxane

186258-72-0

Post Buying Request

Basic information

Product Name: (2R,4S,5R)-5-Allyloxy-2-(4-methoxy-phenyl)-4-pent-4-enyl-[1,3]dioxane
Synonyms: (2R,4S,5R)-5-Allyloxy-2-(4-methoxy-phenyl)-4-pent-4-enyl-[1,3]dioxane
CAS NO:186258-72-0
Molecular Formula:
Molecular Weight: 318.413
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: (2R,4S,5R)-5-Allyloxy-2-(4-methoxy-phenyl)-4-pent-4-enyl-[1,3]dioxane(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S,5R)-5-Allyloxy-2-(4-methoxy-phenyl)-4-pent-4-enyl-[1,3]dioxane(186258-72-0)
EPA Substance Registry System: (2R,4S,5R)-5-Allyloxy-2-(4-methoxy-phenyl)-4-pent-4-enyl-[1,3]dioxane(186258-72-0)

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: 186258-72-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

186258-72-0 Suppliers

Recommended suppliers

186258-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186258-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,2,5 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 186258-72:
(8*1)+(7*8)+(6*6)+(5*2)+(4*5)+(3*8)+(2*7)+(1*2)=170
170 % 10 = 0
So 186258-72-0 is a valid CAS Registry Number.

186258-72-0Upstream product

186258-72-0Downstream Products

186258-72-0Relevant academic research and scientific papers

Enantioselective synthesis of medium-ring sub-units of brevetoxin A by ring-closing metathesis

Clark, J. Stephen,Kettle, Jason G.

, p. 127 - 130 (2007/10/03)

A new strategy for the enantioselective synthesis of eight- and nine-membered cyclic ethers corresponding to sub-units of brevetoxin A has been developed. The strategy involves the use of ring-closing metathesis reactions of allylic ethers to effect ring construction.

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 186258-72-0