Cas 86397-86-6,diethyl 1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate

86397-86-6

Post Buying Request

Basic information

Product Name: diethyl 1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate
Synonyms: diethyl 1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate
CAS NO:86397-86-6
Molecular Formula:
Molecular Weight: 349.814
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: diethyl 1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate(86397-86-6)
EPA Substance Registry System: diethyl 1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate(86397-86-6)

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: 86397-86-6(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

86397-86-6 Suppliers

Recommended suppliers

86397-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86397-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,9 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86397-86:
(7*8)+(6*6)+(5*3)+(4*9)+(3*7)+(2*8)+(1*6)=186
186 % 10 = 6
So 86397-86-6 is a valid CAS Registry Number.

86397-86-6Upstream product

86397-86-6Downstream Products

86397-86-6Relevant academic research and scientific papers

Hypervalent iodine in synthesis. 62: A tandem dimerization-cyclocondensation of enamine-esters with [bis(trifluoroacetoxy)iodo]benzene: A method of synthesis of highly substituted pyrroles

Zhang,Chen

, p. 1619 - 1624 (2001)

A tandem dimerization-cyclocondensation of enamine-esters with [bis(trifluoroacetoxy)iodo]benzene(BTI) provides an effective method for synthesis of highly substituted pyrroles.

Manganese (III) acetate mediated synthesis of polysubstituted pyrroles under solvent-free ball milling

Zeng, Ji-Chao,Xu, Hui,Yu, Fei,Zhang, Ze

supporting information, p. 674 - 678 (2017/01/25)

Under solvent-free ball milling conditions, a simple and mild method was developed for efficient synthesis of 2,5-dimethyl-3,4-dicarboxylate-pyrroles and N-substituted 3,4-diphenylpyrroles via condensation-annulation of amines with acetoacetate and 2-phen

Synthesis of polysubstituted pyrroles via phi(OAC)2-mediated oxidative coupling of enamine esters and ketones

Wang, Jun-Yan,Liu, Su-Ping,Yu, Wei

experimental part, p. 2529 - 2533 (2010/02/28)

Enamine esters or ketones could undergo homocoupling by the action of (diacetoxyiodo)benzene in the presence of BF3OEt2, giving rise to pyrrole products. This reaction could be used to synthesize symmetric polysubstituted pyrroles. Some asymmetric polysub

OXIDATION OF ENAMINE-ESTERS WITH LEAD TETRA-ACETATE - PART 3. β-AMINOCINNAMATES AND β-AMINOCROTONATES

Sukari, Mohamed A.,Vernon, John M.

, p. 793 - 796 (2007/10/02)

Oxidation of β-aminocinnamates and β-aminocrotonates with lead tetra-acetate gives fully substituted pyrrole-3,4-diesters.

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 86397-86-6