Cas 163000-06-4,6,7-dihydro-5H-Pyrrolo[1,2-a]iMidazole-3-carboxylic acid ethyl ester

163000-06-4

Post Buying Request

Basic information

Product Name: 6,7-dihydro-5H-Pyrrolo[1,2-a]iMidazole-3-carboxylic acid ethyl ester
Synonyms: 6,7-dihydro-5H-Pyrrolo[1,2-a]iMidazole-3-carboxylic acid ethyl ester;ethyl 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole-3-carboxylate
CAS NO:163000-06-4
Molecular Formula: C9H12N2O2
Molecular Weight: 180.20378
EINECS: N/A
Product Categories: N/A
Mol File: 163000-06-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6,7-dihydro-5H-Pyrrolo[1,2-a]iMidazole-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6,7-dihydro-5H-Pyrrolo[1,2-a]iMidazole-3-carboxylic acid ethyl ester(163000-06-4)
EPA Substance Registry System: 6,7-dihydro-5H-Pyrrolo[1,2-a]iMidazole-3-carboxylic acid ethyl ester(163000-06-4)

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: 163000-06-4(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

163000-06-4 Suppliers

Recommended suppliersmore

163000-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163000-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,0,0 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 163000-06:
(8*1)+(7*6)+(6*3)+(5*0)+(4*0)+(3*0)+(2*0)+(1*6)=74
74 % 10 = 4
So 163000-06-4 is a valid CAS Registry Number.

163000-06-4Upstream product

163000-06-4Downstream Products

163000-06-4Relevant articles and documents

Transformation of Alkyl N-(Vinyloxy)benzimidates to Alkyloxazoles. Mechanism and Extension

Yokoyama, Masataka,Menjo, Yasuhiro,Ubukata, Makoto,Irie, Masakazu,Watanabe, Mikari,Togo, Hideo

, p. 2219 - 2226 (1994)

Transformation of alkyl N-(vinyloxy)benzimidates to alkyloxazoles proceeds through the intermediates: a charge-separated 1,2-oxazetidine derivative and then 1-hydroxy-2-imino>maleic acid diester, while their photochemical transformation takes place via a concerted sigmatropic shift.As the extension of this reaction, the preparation of the precursor proposed for virginiamycin M2 synthesis and the reaction of N-analogs of alkyl N-(vinyloxy)benzimidates are described.

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 163000-06-4