Cas 6925-51-5,2-Butenedioic acid, 2-(1-cyclohexen-1-ylphenylamino)-, dimethyl ester, (Z)-

6925-51-5

Post Buying Request

Basic information

Product Name: 2-Butenedioic acid, 2-(1-cyclohexen-1-ylphenylamino)-, dimethyl ester, (Z)-
Synonyms:
CAS NO:6925-51-5
Molecular Formula: C18H21NO4
Molecular Weight: 315.369
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: 2-Butenedioic acid, 2-(1-cyclohexen-1-ylphenylamino)-, dimethyl ester, (Z)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Butenedioic acid, 2-(1-cyclohexen-1-ylphenylamino)-, dimethyl ester, (Z)-(6925-51-5)
EPA Substance Registry System: 2-Butenedioic acid, 2-(1-cyclohexen-1-ylphenylamino)-, dimethyl ester, (Z)-(6925-51-5)

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: 6925-51-5(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

6925-51-5 Suppliers

Recommended suppliers

6925-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6925-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6925-51:
(6*6)+(5*9)+(4*2)+(3*5)+(2*5)+(1*1)=115
115 % 10 = 5
So 6925-51-5 is a valid CAS Registry Number.

6925-51-5Upstream product

6925-51-5Downstream Products

6925-51-5Relevant academic research and scientific papers

CONDENSATION OF AZOMETHINES WITH DIMETHYL ACETYLENEDICARBOXYLATE

Prostakov, N. S.,Gaivoronskaya, L. A.,Zakharov, V. F.,Kuznetsov, V. V.,Das, S. K.,Aliev, A. E.

, p. 295 - 300 (2007/10/02)

The condensation of dimethyl acetylenedicarboxylate with benzylidene- and cyclohexylideneaniline, as well as with cyclohexylidene-p-toluidine and cyclohexylidene-p-anisidine, under various conditions gave 1:1, 1:2, and 1:3 adducts.The structures of the isolated substances, which are formed as a result of the addition of the ester to the azomethines with subsequent 1,5-prototropic rearrangement (arylcyclohexenylvinylamines), as well as by cycloaddition (substituted dihydropyridines and spiro-cyclohexanedihydropyridines), are discussed.

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 6925-51-5