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methyl (3R,4R,4aS)-7-[(5R,6R,10aS)-1,5,9-trihydroxy-10a-methoxycarbonyl-6-methyl-8-oxo-6,7-dihydro-5H-xanthen-2-yl]-4,8,9-trihydroxy-3-methyl-1-oxo-3,4-dihydro-2H-xanthene-4a-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51152-25-1

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51152-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51152-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,5 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51152-25:
(7*5)+(6*1)+(5*1)+(4*5)+(3*2)+(2*2)+(1*5)=81
81 % 10 = 1
So 51152-25-1 is a valid CAS Registry Number.

51152-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name secalonic acid E

1.2 Other means of identification

Product number -
Other names (5R,6R,10aS,5'R,6'R,10'aS)-1,5,8,1',5',8'-Hexahydroxy-6,6'-dimethyl-9,9'-dioxo-5,6,7,9,5',6',7',9'-octahydro-[2,2']bixanthenyl-10a,10'a-dicarboxylic acid dimethyl ester

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:51152-25-1 SDS

51152-25-1Upstream product

51152-25-1Downstream Products

51152-25-1Relevant academic research and scientific papers

Syntheses of Dimeric Tetrahydroxanthones with Varied Linkages: Investigation of "shapeshifting" Properties

Qin, Tian,Iwata, Takayuki,Ransom, Tanya T.,Beutler, John A.,Porco, John A.

, p. 15225 - 15233 (2015)

The 2,4′- and 4,4′-linked variants of the cytotoxic agent secalonic acid A and their analogues have been synthesized. Kinetic resolution of an unprotected tetrahydroxanthone scaffold followed by copper-mediated biaryl coupling allowed for efficient access to these compounds. Evaluation of the "shapeshifting" properties of 2,2′-, 2,4′-, and 4,4′-linked variants of the secalonic acids A in a polar solvent in conjunction with assays of the compounds against select cancer cell lines was conducted to study possible correlations between linkage variation and cytotoxicity.

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