Cas 140840-33-1,2-(acetylamino-4,5-dimethylphenylcarbamoyl)-3-(1,2,3-tri-O-acetyl-D-erythro-glycerol-1-yl)-6,7-dimethylquinoxaline

140840-33-1

Post Buying Request

Basic information

Product Name: 2-(acetylamino-4,5-dimethylphenylcarbamoyl)-3-(1,2,3-tri-O-acetyl-D-erythro-glycerol-1-yl)-6,7-dimethylquinoxaline
Synonyms:
CAS NO:140840-33-1
Molecular Formula:
Molecular Weight: 578.622
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-(acetylamino-4,5-dimethylphenylcarbamoyl)-3-(1,2,3-tri-O-acetyl-D-erythro-glycerol-1-yl)-6,7-dimethylquinoxaline(CAS DataBase Reference)
NIST Chemistry Reference: 2-(acetylamino-4,5-dimethylphenylcarbamoyl)-3-(1,2,3-tri-O-acetyl-D-erythro-glycerol-1-yl)-6,7-dimethylquinoxaline(140840-33-1)
EPA Substance Registry System: 2-(acetylamino-4,5-dimethylphenylcarbamoyl)-3-(1,2,3-tri-O-acetyl-D-erythro-glycerol-1-yl)-6,7-dimethylquinoxaline(140840-33-1)

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: 140840-33-1(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

140840-33-1 Suppliers

Recommended suppliers

140840-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140840-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,4 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140840-33:
(8*1)+(7*4)+(6*0)+(5*8)+(4*4)+(3*0)+(2*3)+(1*3)=101
101 % 10 = 1
So 140840-33-1 is a valid CAS Registry Number.

140840-33-1Upstream product

140840-33-1Downstream Products

140840-33-1Relevant academic research and scientific papers

Mode of formation of quinoxaline versus 2[1H]-quinoxalin-one rings from dehydro-D-erythorbic acid

Mousaad,Rashed,Hamid,El Kilany,Sayed,El Ashry

, p. 59 - 66 (2007/10/02)

The mode of formation of the quinoxaline versus 2[1H]-quinoxalinone rings by the reaction of o-diamines with dehydro-D-erythorbic acid has been investigated. The study was carried out by using one and two molar equivalents of 1,2-diamino-4,5-dimethylbenze

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 140840-33-1