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1061-93-4

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1061-93-4 Usage

Family

Chromene

Class

Chromones

Properties

Two acetyl groups attached to a phenyl ring and a chromene backbone

Uses

Commonly used in organic synthesis and pharmaceutical research

Value

Unique structure and reactivity make it valuable in the creation of new molecules with desired biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 1061-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1061-93:
(6*1)+(5*0)+(4*6)+(3*1)+(2*9)+(1*3)=54
54 % 10 = 4
So 1061-93-4 is a valid CAS Registry Number.

1061-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-acetyloxy-4-(5,7-diacetyloxy-4-oxochromen-2-yl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 3',4',5,7-tetra-O-acetylluteolin

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:1061-93-4 SDS

1061-93-4Relevant articles and documents

Isolation, chemical analysis, and study of the hypolipidemic activity of the total flavonoid extract from thermopsis altherniaflora

Khushbaktova,Faizieva,Syrov,Yuldashev,Batirov,Mamatkhanov

, p. 155 - 158 (2001)

-

Flavonoids from the aerial part of Vicia subvillosa

Yuldashev

, p. 99 - 100 (2005)

-

Flavonoids and coumarins from Allium rotundum

Maisashvili,Gvazava,Kuchukhidze

, p. 87 - 88 (2009)

-

Extraction, Isolation and Characterization of Valuable Worked on Acacia Tortilis

Muhaisen, Hasan M. H.

, p. 6731 - 6747 (2021/11/01)

Acacia tortilis is one of the important species of genus Acacia belonging to family Leguminaceae. Though there is no more study performed on this plant but it plays important role in the countries where it found. These countries include North Africa, Arabian Peninsula and Asian countries. The various part of Acacia tortilis plant say leaves, pods, gum exudates and bark were used as antidiabetic, antidiarrhoeal, antiasthmatic and also had several other medicinal benefits. The present discussion deals with the isolation and characterization of the following compounds from the leaves of Acacia tortilis. Lupan-3-ol, 12,20-diene, Lupan-12, 20-dien 3-one, Friedelin, ?-amyrin, ?- sitosterol, Apigenin, Luteolin, Quercetin, 5,7-dihydroxy-4-p-methyl benzylisoflavone, Vitexin, 2',6'-dihydroxy chalcone-4'-O-glucoside.

Synthesis, characterization, anti-inflammatory and anti-proliferative activity against MCF-7 cells of O-alkyl and O-acyl flavonoid derivatives

Hoang, T. Kim-Dung,Huynh, T. Kim-Chi,Nguyen, Thanh-Danh

, p. 45 - 52 (2015/10/12)

A series of O-alkyl and O-acyl flavonoid derivatives was synthesized in high efficiency. Alkylation and acylation of 5-hydroxyflavonoids showed that the low reactivity hydroxyl group, 5-OH, well reacted with strong reagents whereas with weaker reagents, the different products were obtained dependently on structural characteristic of ring C of respective flavonoid. In order to evaluate anti-inflammatory activity, all compounds were tested for in vitro inhibition of bovine serum albumin denaturation and in vivo inhibition of carrageenan-induced mouse paw edema. Among them, the compounds 3, 3b, 4b and 4c demonstrated more effective anti-inflammatory activity than standard drugs (diclofenac sodium and ketoprofen) in both tests. Meanwhile, the flavonoids 2, 2c, 3a and 4b displayed anti-proliferative activity against MCF-7 cell lines. Triacetyl derivative of hesperetin 4b inducing degradation of DNA in MCF-7 cells was observed.

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