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1237605-01-4

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1237605-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1237605-01-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,7,6,0 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1237605-01:
(9*1)+(8*2)+(7*3)+(6*7)+(5*6)+(4*0)+(3*5)+(2*0)+(1*1)=134
134 % 10 = 4
So 1237605-01-4 is a valid CAS Registry Number.

1237605-01-4SDS

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 6-methoxy-7-hydroxy-4'-O-β-D-glucosylisoflavone

1.2 Other means of identification

Product number -
Other names .glycitein-4'-O-β-D-glucoside

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:1237605-01-4 SDS

1237605-01-4Downstream Products

1237605-01-4Relevant articles and documents

Synthesis of β-maltooligosaccharides of glycitein and daidzein and their anti-oxidant and anti-allergic activities

Shimoda, Kei,Hamada, Hiroki

, p. 5153 - 5161 (2010)

The production of β-maltooligosaccharides of glycitein and daidzein using Lactobacillus delbrueckii and cyclodextrin glucanotransferase (CGTase) as biocatalysts was investigated. The cells of L. delbrueckii glucosylated glycitein and daidzein to give their corresponding 4′- and 7-O-β-glucosides. The β-glucosides of glycitein and daidzein were converted into the corresponding β-maltooligosides by CGTase. The 7-O-β- glucosides of glycitein and daidzein and 7-O-β-maltoside of glycitein showed inhibitory effects on IgE antibody production. On the other hand, β-glucosides of glycitein and daidzein exerted 2,2-diphenyl-1- picrylhydrazyl (DPPH) free-radical scavenging activity and supeoxide-radical scavenging activity.

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