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23982-44-7

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23982-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23982-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,8 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23982-44:
(7*2)+(6*3)+(5*9)+(4*8)+(3*2)+(2*4)+(1*4)=127
127 % 10 = 7
So 23982-44-7 is a valid CAS Registry Number.

23982-44-7SDS

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-(3',4'-dimethoxyphenyl)-7-methoxycoumarin

1.2 Other means of identification

Product number -
Other names 7-methoxy-4-(3,4-dimethoxyphenyl)coumarin

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:23982-44-7 SDS

23982-44-7Relevant articles and documents

Synthesis and NMR of 4-Aryl-3,4-dihydrocoumarins and 4-arylcoumarins

Sun, Jie,Wang, Yanfeng

, p. 7753 - 7758 (2015/02/02)

This paper described the synthesis and 1H and 13C NMR chemical shifts of a series of 4-aryl-3,4-dihydrocoumarin and 4-arylcoumarin derivatives based on a combination of 1H and 13C NMR, HSQC and HMBC experiments.

Efficient synthesis and biological evaluation of 4-arylcoumarin derivatives

Sun, Jie,Ding, Wei Xian,Zhang, Ke Yun,Zou, Yong

scheme or table, p. 667 - 670 (2012/01/13)

Two bioactive natural 4-arylcoumarins, 5,7,4′-trimethoxy-4- phenylcoumarin (1a), 5,7-dimethoxy-4-phenylcoumarin (1b) and five closely related derivatives 1c-g were synthesized. In vitro evaluation with a catechol subunit for antioxidant and antimicrobial activity, these compounds using standard methods showed that compounds 1d, 1f displayed promise radical scavenging activity and 1f was found to be the most active one against Bacillus dysenteriae.

VOLUBOLIN, A 4-PHENYL-2H-1-BENZOPYRAN-2ONE FROM DALBERGIA VOLUBILIS

Chawla, H. Mohindra,Mittal, Ram S.

, p. 2625 - 2626 (2007/10/02)

From the ether soluble portion of a methanolic extract of young non-green branches of Dalbergia volubilis, sitosterol, 7-hydroxy-4-methyl-2H-1-benzopyran-2-one, dalbergin, p-hydroxy cinnamic acid, biochanin-A and a new 4-phenylcoumarin, volubolin, have been isolated.The structure of volubolin as 7-hydroxy-4-(3-hydroxy-4-methoxy-phenyl)-2H-1-benzopyran-2-one has been established on the basis of spectral and chemical evidence.Cooccurrence of 4-methyl- and 4-phenyl-coumarins with isoflavones is of biogenetic interest. - Key Word Index: Dalbergia volubilis; Leguminosae; young branches; 7-hydroxy-4-methyl coumarin; dalbergin; biochanin-A; 7-hydroxy-4-(3-hydroxy-4-methoxyphenyl)-2H-1-benzopyran-2-one.

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