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1-(2-QUINOXALINYL)-1,2,3,4-BUTANETETROL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80840-09-1

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80840-09-1 Usage

Chemical Properties

Light Brown Solid

Check Digit Verification of cas no

The CAS Registry Mumber 80840-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,4 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80840-09:
(7*8)+(6*0)+(5*8)+(4*4)+(3*0)+(2*0)+(1*9)=121
121 % 10 = 1
So 80840-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O4/c15-6-10(16)12(18)11(17)9-5-13-7-3-1-2-4-8(7)14-9/h1-5,10-12,15-18H,6H2

80840-09-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-quinoxalin-2-ylbutane-1,2,3,4-tetrol

1.2 Other means of identification

Product number -
Other names 1-(quinoxalin-2-yl)butane-1,2,3,4-tetrol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80840-09-1 SDS

80840-09-1Relevant academic research and scientific papers

Degradation of glucose: reinvestigation of reactive α-dicarbonyl compounds

Jenny, Gobert,Glomb, Marcus A.

experimental part, p. 8591 - 8597 (2010/07/15)

Maillard reactions influence the formation of flavor and color in processed foods in an important way. Reducing sugars and amino acids ultimately react to stable end products. To elucidate the complex formation pathways a vast number of experiments have b

Quinoxalines Derived from D-Galactose and o-Phenylenediamine in Acidic Media

Morita, Naofumi,Inoue, Keiichi,Takagi, Masanosuke

, p. 1329 - 1332 (2007/10/02)

Quinoxalines derived from D-galactose with o-phenylenediamine (OPD) in acidic media under reflux were studied by using GLC and NMR measurements.Four quinoxaline derivatives were obtained from the reaction mixture, and were identical with those derived from D-glucose.The yields of 2-(D-lyxo-tetrahydroxybutyl)quinoxaline (GA-III), and the stereoisomeric derivative of GA-III, i.e., 2-(D-arabino-tetrahydroxybutyl)quinoxaline (ATBQ), were 13.2 and 5.3percent, respectively.The ratio of GA-III to ATBQ derived from D-galactose was reciprocally coincident with that from D-glucose.Some proposals are made on the relationship between the isomerization of these sugars and the formation of quinoxaline derivatives.

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