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(E)-1-[2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)benzofuran-7-yl]-3-phenyl-2-propen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84435-29-0

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84435-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84435-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,3 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84435-29:
(7*8)+(6*4)+(5*4)+(4*3)+(3*5)+(2*2)+(1*9)=140
140 % 10 = 0
So 84435-29-0 is a valid CAS Registry Number.

84435-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-Flemistrictin

1.2 Other means of identification

Product number -
Other names flemistrictin-E

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:84435-29-0 SDS

84435-29-0Downstream Products

84435-29-0Relevant academic research and scientific papers

Synthesis of (+/-)-Flemistrictin-E and Flemistrictin-F

Vemuri, V. S. S.,Rao, C. P.,Rao, J. Madhusudhana,Rao, K. V. Jagannadha

, p. 1122 - 1123 (2007/10/02)

(+/-)-Flemistrictin-E (I) has been synthesised by selective acetylation of the non-chelated hydroxyl of 3-C-prenylresacetophenone (III), treatment of the resulting IV with perbenzoic acid at 0 deg C in dry ether followed by chalcone condensation of the resulting ketone (V) with benzaldehyde. (+/-)-Flemistrictin-F (II) has been synthesised by treating 4-O-acetyl-3-C-prenylresacetophenone (IV) with perbenzoic acid in dry chloroform in the presence of p-toluenesulphonic acid followed by chalcone condensation of the resulting ketone (VI) with benzaldehyde.

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