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53580-72-6

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53580-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53580-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,8 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53580-72:
(7*5)+(6*3)+(5*5)+(4*8)+(3*0)+(2*7)+(1*2)=126
126 % 10 = 6
So 53580-72-6 is a valid CAS Registry Number.

53580-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-5-hydroxymethyl-3-acetoxypyridine

1.2 Other means of identification

Product number -
Other names 3-acetoxy-5-hydroxymethyl-2,4-dimethyl-pyridine

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:53580-72-6 SDS

53580-72-6Relevant articles and documents

Preparation and investigation of vitamin B6-derived aminopyridinol antioxidants

Serwa, Remigiusz,Nam, Tae-Gyu,Valgimigli, Luca,Culbertson, Sean,Rector, Christopher L.,Jeong, Byeong-Seon,Pratt, Derek A.,Porter, Ned A.

supporting information; experimental part, p. 14106 - 14114 (2011/02/22)

3-Pyridinols bearing amine substitution para to the hydroxylic moiety have previously been shown to inhibit lipid peroxidation more effectively than typical phenolic antioxidants, for example, α-tocopherol. We report here high-yielding, large-scale syntheses of mono- and bicyclic aminopyridinols from pyridoxine hydrochloride (i.e., vitamin B6). This approach provides straightforward, scaleable access to novel, potent, molecular scaffolds whose antioxidant properties have been investigated in homogeneous solutions and in liposomal vesicles. These molecular aggregates mimic cell membranes that are the targets of oxidative damage in vivo.

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