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4',6'-Dihydroxy-3'-(3-methyl-2-butenyl)-2'-methoxyacetophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27364-64-3

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27364-64-3 Usage

Preparation

Preparation by prenylation of 2,4-dihydroxy-6- methoxy-acetophenone with 2-methyl-3-buten- 2-ol in the presence of boron trifluoride etherate.

Check Digit Verification of cas no

The CAS Registry Mumber 27364-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,6 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27364-64:
(7*2)+(6*7)+(5*3)+(4*6)+(3*4)+(2*6)+(1*4)=123
123 % 10 = 3
So 27364-64-3 is a valid CAS Registry Number.

27364-64-3SDS

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 2,4-dihydroxy-5-prenyl-6-methoxy-acetophenone

1.2 Other means of identification

Product number -
Other names Acronylin

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:27364-64-3 SDS

27364-64-3Relevant academic research and scientific papers

Total Synthesis and in Vitro Anti-Tumor-Promoting Activities of Racemic Acetophenone Monomers from Acronychia trifoliolata

Morita, Chihiro,Kobayashi, Yukiko,Saito, Yohei,Miyake, Katsunori,Tokuda, Harukuni,Suzuki, Nobutaka,Ichiishi, Eiichiro,Lee, Kuo-Hsiung,Nakagawa-Goto, Kyoko

, p. 2890 - 2897 (2016/12/07)

Six acetophenone derivatives, acronyculatins I (1), J (2), K (3), L (4), N (5), and O (6), were recently isolated from Acronychia trifoliolata, and the structure of the known acronyculatin B (7) was revised. Because of the limited quantities of isolated p

AN ELEGANT SYNTHESIS OF SOME NATURALLY OCCURRING LINEAR ACETYLCHROMENES: EUPATORIOCHROMENE, METHYLEUPATORIOCHROMENE (ENCECALIN); EVODIONOL AND METHYLEVODIONOL

Ahluwalia, V. K.,Prakash, Chandra,Gupta, Ranjna

, p. 609 - 611 (2007/10/02)

An elegant synthesis of linear acetylchromenes, viz eupatoriochromene, methyleupatoriochromene (encecalin), evodionol and methylevodionol, has been achieved by blocking the reactive position C-3 of the appropriate ketones with an iodo group, prenylation with 3-chloro-3-methylbut-1-yne and subsequent cyclisation.Regiospecific introduction of C-prenyl group in the less reactive position C-5 has been achieved by the reaction of the appropriate 3-iodo ketones with 2-methylbut-3-en-2-ol.The 5-prenyl ketones are also essential intermediates for the synthesis of linear acetylchromenes.

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