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26103-97-9

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26103-97-9 Usage

General Description

1-Butanone, 3-methyl-1-(2,4,6-trihydroxyphenyl)-, also known as 3-Methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one, is a chemical compound with the molecular formula C11H14O4. It is a derivative of butanone and contains a phenolic group with three hydroxyl substituents. 1-Butanone, 3-methyl-1-(2,4,6-trihydroxyphenyl)- is often used as a flavoring and fragrance ingredient due to its pleasant and sweet aroma. It is also used in the production of various pharmaceuticals and as a chemical intermediate in organic synthesis. Additionally, it has been studied for its potential antioxidant and antimicrobial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 26103-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,0 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26103-97:
(7*2)+(6*6)+(5*1)+(4*0)+(3*3)+(2*9)+(1*7)=89
89 % 10 = 9
So 26103-97-9 is a valid CAS Registry Number.

26103-97-9SDS

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 3-methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one

1.2 Other means of identification

Product number -
Other names isovaleroyl phloroglucinole

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:26103-97-9 SDS

26103-97-9Relevant articles and documents

Rhodomentosones A and B: Two Pairs of Enantiomeric Phloroglucinol Trimers from Rhodomyrtus tomentosa and Their Asymmetric Biomimetic Synthesis

Bai, Yang-Ting-Zhi,Deng, Lu-Ming,Hu, Li-Jun,Huang, Xiao-Jun,Jiang, Ren-Wang,Li, Chuang-Chuang,Li, Yao-Lan,Qin, Guan-Qiu,Song, Qiao-Yun,Su, Jun-Cheng,Tang, Wei,Wang, Jie,Wang, Ying,Ye, Wen-Cai

, p. 4499 - 4504 (2021)

Rhodomentosones A and B (1 and 2), two pairs of novel enantiomeric phloroglucinol trimers featuring a unique 6/5/5/6/5/5/6-fused ring system were isolated from Rhodomyrtus tomentosa. Their structures with absolute configurations were elucidated by NMR spe

Polycyclic benzodifuran compound and application thereof as anti-RSV drug

-

Paragraph 0027, (2021/01/04)

The invention discloses a polycyclic benzodifuran compound with a formula (I), a preparation method thereof and an application of the polycyclic benzodifuran compound as an anti-respiratory syncytialvirus (RSV) drug. The polycyclic benzodifuran compound d

Expedient Synthesis of Lupulones and Their Derivatization to 2,8-7H-Dihydrochromen-7-ones

Blondeel, Eline,D'hooghe, Matthias,Decuyper, Lena,Depetter, Yves,Kaur, Gurkirat,Van Hecke, Kristof,Versyck, Charlotte

, p. 442 - 444 (2020/10/02)

A convenient and improved method for the synthesis of beta acids or lupulones, which are known to possess e. g. anti-cancer, anti-inflammatory, anti-oxidative and antimicrobial activity, has been developed successfully. Further derivatization of these complex structures to the corresponding dihydrochromen-7-ones, including the natural product machuone, was realized to simplify their analysis and to confirm their molecular structure. In addition to practical and safe laboratory procedures, the advantages associated with this new approach involve the use of water as a solvent and the direct crystallization of lupunones from acetonitrile, rendering our strategy more efficient and benign as compared to available methods.

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