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Ethanone, 1-(2,4-dihydroxy-3,5-dimethylphenyl)-, also known as 2,4-Dihydroxy-3,5-dimethylacetophenone, is an organic compound with the chemical formula C10H12O3. It is a derivative of acetophenone, featuring two hydroxyl groups at the 2 and 4 positions, and two methyl groups at the 3 and 5 positions on the phenyl ring. Ethanone, 1-(2,4-dihydroxy-3,5-dimethylphenyl)- is a white crystalline solid and is soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Due to its reactivity and functional groups, it plays a significant role in the chemical industry for the production of various products.

577-45-7

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577-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 577-45-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 577-45:
(5*5)+(4*7)+(3*7)+(2*4)+(1*5)=87
87 % 10 = 7
So 577-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-5-4-8(7(3)11)10(13)6(2)9(5)12/h4,12-13H,1-3H3

577-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-dihydroxy-3,5-dimethylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names Acetylphenone,2',4'-dihydroxy-3',5'-dimethyl

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:577-45-7 SDS

577-45-7Relevant academic research and scientific papers

Biomimetic Total Synthesis of Bisorbicillinol, Bisorbibutenolide, Trichodimerol, and Designed Analogues of the Bisorbicillinoids

Nicolaou,Vassilikogiannakis, Georgios,Simonsen, Klaus B.,Baran, Phil S.,Zhong, Yong-Li,Vidali, Veroniki P.,Pitsinos, Emmanuel N.,Couladouros, Elias A.

, p. 3071 - 3079 (2007/10/03)

The bisorbicillinoids are a growing class of novel natural products endowed with unique biological activity and are associated with fascinating hypotheses for their biosynthesis. A full account of our biomimetic explorations toward the bisorbicillinoids including the total syntheses of bisorbicillinol (1), bisorbibutenolide (2), and trichodimerol (4) from sorbicillin (3) is disclosed. Utilizing the novel dimerization reactions discovered and fine-tuned en route to 1 and 4, several analogues of these natural products have been synthesized. Furthermore, studies on the scope of these novel cycloaddition reactions and the isolation of a number of unexpected products along with proposed mechanisms for their formation are reported. These findings add to our knowledge of the largely unexplored chemistry of o-quinols and related aromatic systems.

SYNTHESIS OF THREE NATURAL 1,3-DIARYLPROPANES: TWO REVISED STRUCTURES

Morais, Anselmo A.,Fo, Raimundo Braz,Fraiz, Silas V. Jr

, p. 239 - 242 (2007/10/02)

1-(2',4'-dihydroxy-3',5'-dimethylphenyl)-3-(2"-hydroxy-4",5"-methylenedioxyphenyl)-Propane, isolated from Iryanthera coriacea and I. laevis, 1-(2'-hydroxy-4'-methoxy-5'-methylphenyl)-3-(2"-hydroxy-4",5"-methylene-dioxyphenyl)-propane, isolated from I. laevis, and 1-(2'-hydroxy-4'-methoxyphenyl)-3-(3"-hydroxy-4"-methoxyphenyl)-propane, isolated from Virola multinervia, were synthesized by processes which involved catalityc hydrogenation of the appropriate chalcones and Clemmensen reduction of dihydrochalcones.Only the structures of 1,3-diarylpropanes isolated from V. multinervia and I. laevis were revised. - Keywords: Virola multinervia; Iryanthera coriaceae; I. laevis; Myristicaceae; 1,3-diarylpropanes; synthesis; reduction of chalcones and dihydrochalcones.

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