Cas 86052-40-6,({[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-amino}-phenyl-methyl)-phosphonic acid diethyl ester

86052-40-6

Post Buying Request

Basic information

Product Name: ({[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-amino}-phenyl-methyl)-phosphonic acid diethyl ester
Synonyms: ({[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-amino}-phenyl-methyl)-phosphonic acid diethyl ester
CAS NO:86052-40-6
Molecular Formula:
Molecular Weight: 365.796
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-(2-Chloro-phenyl)-meth-(E)-ylidene]-amino}-phenyl-methyl)-phosphonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ({[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-amino}-phenyl-methyl)-phosphonic acid diethyl ester(86052-40-6)
EPA Substance Registry System: ({[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-amino}-phenyl-methyl)-phosphonic acid diethyl ester(86052-40-6)

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: 86052-40-6(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

86052-40-6 Suppliers

Recommended suppliers

86052-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86052-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86052-40:
(7*8)+(6*6)+(5*0)+(4*5)+(3*2)+(2*4)+(1*0)=126
126 % 10 = 6
So 86052-40-6 is a valid CAS Registry Number.

86052-40-6Upstream product

86052-40-6Downstream Products

86052-40-6Relevant academic research and scientific papers

PO-Activated Olefination and Conversion of Aldehydes and Ketones to Higher Amines; II. Synthesis of Arylethylamines

Heymes, A.,Chekroun, I.

, p. 245 - 249 (1987)

The transformation of arylcarboxaldehydes and/or - ketones 2 by three different routes into arylethylamines 3 and/or 4 is reported.According to the first route, the intermediate iminophosphonates 9 react through a classical PO-activated olefination.The second and the third involve the rearrangement of the iminophosphonates 9 into the vinylphosphoramidates 12.

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 86052-40-6