Cas 677315-72-9,2-amino-6-(4-chloro-phenyl)-4-ethyl-6<i>H</i>-[1,3]thiazine-5-carboxylic acid methyl ester

677315-72-9

Post Buying Request

Basic information

Product Name: 2-amino-6-(4-chloro-phenyl)-4-ethyl-6H-[1,3]thiazine-5-carboxylic acid methyl ester
Synonyms: 2-amino-6-(4-chloro-phenyl)-4-ethyl-6H-[1,3]thiazine-5-carboxylic acid methyl ester
CAS NO:677315-72-9
Molecular Formula:
Molecular Weight: 310.804
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-amino-6-(4-chloro-phenyl)-4-ethyl-6H-[1,3]thiazine-5-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-6-(4-chloro-phenyl)-4-ethyl-6H-[1,3]thiazine-5-carboxylic acid methyl ester(677315-72-9)
EPA Substance Registry System: 2-amino-6-(4-chloro-phenyl)-4-ethyl-6H-[1,3]thiazine-5-carboxylic acid methyl ester(677315-72-9)

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: 677315-72-9(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

677315-72-9 Suppliers

Recommended suppliers

677315-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 677315-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,3,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 677315-72:
(8*6)+(7*7)+(6*7)+(5*3)+(4*1)+(3*5)+(2*7)+(1*2)=189
189 % 10 = 9
So 677315-72-9 is a valid CAS Registry Number.

677315-72-9Upstream product

677315-72-9Downstream Products

677315-72-9Relevant academic research and scientific papers

Combinatorial Synthesis of Functionalized 1,3-Thiazine Libraries Using a Combined Polymer-Supported Reagent/Catch-and-Release Strategy

Strohmeier, Gernot A.,Kappe, C. Oliver

, p. 621 - 624 (2007/10/03)

A dual role: The supported sulfonic acid reagent promotes the ring closure of the thiazine products and also binds them in situ as ion pairs (see scheme). The nonbasic by-products and excess reagents can be removed by filtration and the products subsequen

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 677315-72-9