Cas 960505-53-7,(E)-2-[3-(4-chlorophenyl)prop-2-enoyl]phenyl nonafluorobutanesulfonate

960505-53-7

Post Buying Request

Basic information

Product Name: (E)-2-[3-(4-chlorophenyl)prop-2-enoyl]phenyl nonafluorobutanesulfonate
Synonyms: (E)-2-[3-(4-chlorophenyl)prop-2-enoyl]phenyl nonafluorobutanesulfonate
CAS NO:960505-53-7
Molecular Formula:
Molecular Weight: 540.791
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: (E)-2-[3-(4-chlorophenyl)prop-2-enoyl]phenyl nonafluorobutanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-[3-(4-chlorophenyl)prop-2-enoyl]phenyl nonafluorobutanesulfonate(960505-53-7)
EPA Substance Registry System: (E)-2-[3-(4-chlorophenyl)prop-2-enoyl]phenyl nonafluorobutanesulfonate(960505-53-7)

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: 960505-53-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

960505-53-7 Suppliers

Recommended suppliers

960505-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960505-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,5,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 960505-53:
(8*9)+(7*6)+(6*0)+(5*5)+(4*0)+(3*5)+(2*5)+(1*3)=167
167 % 10 = 7
So 960505-53-7 is a valid CAS Registry Number.

960505-53-7Upstream product

960505-53-7Downstream Products

960505-53-7Relevant academic research and scientific papers

Synthesis of chiral 3-substituted indanones via an enantioselective reductive-heck reaction

Minatti, Ana,Zheng, Xiaolai,Buchwald, Stephen L.

, p. 9253 - 9258 (2008/03/13)

(Chemical Equation Presented) An efficient intramolecular palladium-catalyzed, asymmetric reductive-Heck reaction has been developed, which allowed for the synthesis of either enantiomerically enriched 3-substituted indanones or α-exo-methylene indanones depending on the base used.

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 960505-53-7