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32764-43-5

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32764-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32764-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32764-43:
(7*3)+(6*2)+(5*7)+(4*6)+(3*4)+(2*4)+(1*3)=115
115 % 10 = 5
So 32764-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO5/c7-3-4(10)5(2(9)1-8)12-6(3)11/h2,5,8-9,11H,1,7H2

32764-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-2-(1,2-dihydroxyethyl)-3-hydroxy-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names Amino reductone

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:32764-43-5 SDS

32764-43-5Downstream Products

32764-43-5Relevant articles and documents

Antioxidant activity and Neurite outgrowth-enhancing activity of scorbamic acid and a red pigment derived from ascorbic acid

Ikeda, Nao,Ito, Hideyuki,Iwaoka, Yuji,Ohno, Asako,Tai, Akihiro

, p. 838 - 842 (2020)

L-Ascorbic acid (AA), known as vitamin C, can form browning products by a non-enzymatic process during storage and the browning products cause deterioration of agricultural products. In the browning reaction, a red pigment, 2,2′-nitrilodi-2(2′)-deoxy-L-ascorbic acid ammonium salt (NDA), is generated from AA viaL-scorbamic acid (SCA) as an intermediate. However, the biological activities of SCA and NDA have not yet been clarified. In this study, we assayed the antioxidant activities of SCA and NDA using ABTS radical cation and their neurite outgrowth-enhancing activities in PC12 cells. SCA showed stronger radical-scavenging activity than that of AA, while NDA hardly showed any activity. SCA and NDA enhanced the neurite outgrowth induced by dibutyryl cyclic AMP after their incorporation into cells in the same manner as that of AA. The results indicated that SCA has antioxidant activity and that SCA and NDA have neurite outgrowth-enhancing activity.

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