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69120-07-6

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69120-07-6 Usage

General Description

Moracin D is a chemical compound found in the Morus alba plant, commonly known as the white mulberry. It belongs to a group of organic compounds called flavonoids, which are known for their antioxidant and anti-inflammatory properties. Moracin D has been studied for its potential pharmacological effects, including its ability to inhibit the growth of cancer cells, reduce inflammation, and regulate blood sugar levels. It has also been shown to have anti-allergic and neuroprotective effects, making it a compound of interest in the field of natural medicine and drug discovery.Overall, Moracin D shows promise as a potential therapeutic agent for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 69120-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,2 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69120-07:
(7*6)+(6*9)+(5*1)+(4*2)+(3*0)+(2*0)+(1*7)=116
116 % 10 = 6
So 69120-07-6 is a valid CAS Registry Number.

69120-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(6-Hydroxy-1-benzofuran-2-yl)-2,2-dimethyl-2H-chromen-5-ol

1.2 Other means of identification

Product number -
Other names -

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:69120-07-6 SDS

69120-07-6Downstream Products

69120-07-6Relevant articles and documents

Functional group manoeuvring for tuning stability and reactivity: Synthesis of cicerfuran, moracins (D, E, M) and chromene-fused benzofuran-based natural products

Rao, Maddali L. N.,Murty, Venneti N.,Nand, Sachchida

, p. 9415 - 9423 (2017/11/23)

The protecting group manoeuvring as a strategy was applied for tuning the stability and reactivity of 4-(2,2-dibromovinyl)benzene-1,3-diol (12a) and 6-(2,2-dibromovinyl)-2,2-dimethylchroman-7-ol (22) in the domino synthesis of benzofuran-based natural products (1-8). The functional group demands and their impact on the reactivity driven by electronic effects were successfully managed by varying the protecting groups with substituted gem-dibromovinylphenols in domino couplings and triarylbismuth reagents under palladium-catalyzed conditions. This approach paved the way for the synthesis of moracin M (1) and cicerfuran (2), and the first time synthesis of moracin D (3) and moracin E (4) along with chromene-fused benzofuran-based natural products (5-8) in overall good yields.

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