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1-Butanone, 3-methyl-1-[2,4,6-trihydroxy-3-(3-methylbutyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26104-01-8

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26104-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26104-01-8 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 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26104-01:
(7*2)+(6*6)+(5*1)+(4*0)+(3*4)+(2*0)+(1*1)=68
68 % 10 = 8
So 26104-01-8 is a valid CAS Registry Number.

26104-01-8SDS

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-trihydroxy-3-(3-methylbutyl)phenyl]butan-1-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-1-(2,4,6-trihydroxy-3-isopentyl-phenyl)-butan-1-on

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:26104-01-8 SDS

26104-01-8Relevant academic research and scientific papers

Divergent Total Syntheses of Rhodomyrtosones A and B

Gervais, Anais,Lazarski, Kiel E.,Porco, John A.

, p. 9584 - 9591 (2015/10/12)

Herein, we report total syntheses of the tetramethyldihydroxanthene natural product rhodomyrtosone B and the related bis-furan β-triketone natural product rhodomyrtosone A. Nickel-(II)-catalyzed 1,4-conjugate addition of an α-alkylidene-β-dicarbonyl subst

Antifungal Activities of 2,4,6-Trihydroxyacylophenones and Related Compounds

Mizobuchi, Shigeyuki,Sato, Yuko

, p. 719 - 724 (2007/10/02)

The antifungal activities of sixty two 2,4,6-trihydroxyacylophenones and related compounds against Trichophyton spp. and other fungi were investigated to study their structure-activity relationship.It was found that the activities of these compounds were closely related to the length of the acyl and alkyl chains attached to the 1,3,5-trihydroxybenzene moiety.Among the compounds tested, 2,4,6-trihydroxy-3-nonylacetophenone (V-7) showed the highest activity against Trichophyton spp., with MICs being 1.57 μg/ml, and was more active than amphotericin B.

The Synthesis of Some Novel Deoxyhumulone Analogues. Observations on the Air-oxidation of 2',4',6'-Trihydroxy-3'-isopentyl-5'-(3-methylbut-2-enyl)isovalerophenone and its corresponding Humulone Derivatives

Cann, Martin R.,Davis, Anne-Marie,Shannon, Patrick V. R.

, p. 1413 - 1421 (2007/10/02)

Two novel analogues of natural deoxyhumulone have been synthesised: (a) with the 3-methylbutanoyl side chain replaced by benzoyl, and (b) with the dimethylallyl substituents replaced by the cycloheptylidene analogues.Oxidation of these with air gave the c

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