Cas 328-78-9,1-butoxy-3,5-bis(trifluoromethyl)benzene

328-78-9

Post Buying Request

Basic information

Product Name: 1-butoxy-3,5-bis(trifluoromethyl)benzene
Synonyms: 1-butoxy-3,5-bis(trifluoromethyl)benzene
CAS NO:328-78-9
Molecular Formula:
Molecular Weight: 286.217
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: 1-butoxy-3,5-bis(trifluoromethyl)benzene(CAS DataBase Reference)
NIST Chemistry Reference: 1-butoxy-3,5-bis(trifluoromethyl)benzene(328-78-9)
EPA Substance Registry System: 1-butoxy-3,5-bis(trifluoromethyl)benzene(328-78-9)

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: 328-78-9(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

328-78-9 Suppliers

Recommended suppliers

328-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328-78-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 328-78:
(5*3)+(4*2)+(3*8)+(2*7)+(1*8)=69
69 % 10 = 9
So 328-78-9 is a valid CAS Registry Number.

328-78-9Upstream product

328-78-9Downstream Products

328-78-9Relevant academic research and scientific papers

Light-Promoted Nickel Catalysis: Etherification of Aryl Electrophiles with Alcohols Catalyzed by a NiII-Aryl Complex

Cao, Rui,Lai, Chu-Hui,Li, Gang,Liu, Fengyi,Lu, Huan-Huan,Wang, Chao,Xiao, Jianliang,Xue, Dong,Yang, Liu,Zhang, Wei

, p. 12714 - 12719 (2020)

A highly effective C?O coupling reaction of (hetero)aryl electrophiles with primary and secondary alcohols is reported. Catalyzed by a NiII-aryl complex under long-wave UV (390–395 nm) irradiation in the presence of a soluble amine base without any additional photosensitizer, the reaction enables the etherification of aryl bromides and aryl chlorides as well as sulfonates with a wide range of primary and secondary aliphatic alcohols, affording synthetically important ethers. Intramolecular C?O coupling is also possible. The reaction appears to proceed via a NiI–NiIII catalytic cycle.

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 328-78-9