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4-Aminophenyl b-D-Glucuronide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21080-66-0

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21080-66-0 Usage

Chemical Properties

Yellow Solid

Uses

Metabolite of p-Aminophenol

Check Digit Verification of cas no

The CAS Registry Mumber 21080-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21080-66:
(7*2)+(6*1)+(5*0)+(4*8)+(3*0)+(2*6)+(1*6)=70
70 % 10 = 0
So 21080-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO7/c13-5-1-3-6(4-2-5)19-12-9(16)7(14)8(15)10(20-12)11(17)18/h1-4,7-10,12,14-16H,13H2,(H,17,18)/t7-,8-,9-,10?,12-/m0/s1

21080-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,4S,5R,6S)-6-(4-aminophenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Aminophenyl |A-D-Glucopyranosiduronic Acid

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:21080-66-0 SDS

21080-66-0Relevant academic research and scientific papers

Syntheses of sulfated glycopolymers and analyses of their BACE-1 inhibitory activity

Nishimura, Yuri,Shudo, Hiroki,Seto, Hirokazu,Hoshino, Yu,Miura, Yoshiko

, p. 6390 - 6395 (2013)

The glycopolymers for glycosaminoglycan mimic were synthesized, and the inhibitory effects of Alzheimer's β-secretase (BACE-1) were examined. The regio-selective sulfation was conducted on N-acetyl glucosamine (GlcNAc), and the acrylamide derivatives were

Interaction analyses of amyloid β peptide (1-40) with glycosaminoglycan model polymers

Miura, Yoshiko,Mizuno, Hikaru

supporting information; experimental part, p. 1004 - 1009 (2010/12/19)

We synthesized a novel glycopolymer library with 6-sulfo-GlcNAc and glucuronicacid(GlcA) based on the structure of glycosaminoglycans. The molecular weights of the polymers were controlled via living radical polymerization. The interactions of Aβ(1-40)ith glycopolymers were analyzed by inhibition activity of protein aggregation using ThT fluorescence assay, atomic force microscopy observation, and CD spectra. The inhibition activity of Aβ was much affected by the sugar structure and molecular weight of the polymer. The glycopolymers carrying 6-sulfo-GlcNAc showed inhibition activity toward Aβ aggregate, and those with 6-suflo-GlcNAc and GlcA showed the strong inhibition activity. The glycopolymer libraries yielded valuable information about Aβ aggregate with glycosaminoglycans.

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