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26121-57-3

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26121-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26121-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,2 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26121-57:
(7*2)+(6*6)+(5*1)+(4*2)+(3*1)+(2*5)+(1*7)=83
83 % 10 = 3
So 26121-57-3 is a valid CAS Registry Number.

26121-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Desmethylquassin

1.2 Other means of identification

Product number -
Other names 2-hydroxy-12-methoxy-picrasa-2,12-diene-1,11,16-trione

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:26121-57-3 SDS

26121-57-3Relevant articles and documents

Semisynthetic derivatives of quassin

Lang'at, Caroline C.,Watt, Robert A.,Toth, Istvan,Phillipson, J. David

, p. 6841 - 6856 (2007/10/03)

The natural product quassin has been modified in order to produce compounds with potential antimalarial action. The modifications include demethylation, reduction of the keto function, esterification with simple organic acids and - to enhance the uptake through the biological barriers and increase the stability of the compounds - with lipoamino acids.

An Enantioselective Synthesis of (+)-Picrasin B, (+)-Δ2-Picrasin B, and (+)-Quassin from the R-(-) Enantiomer of the Wieland-Miescher Ketone

Kim, Moonsun,Kawada, Kenji,Gross, Raymond S.,Watt, David S.

, p. 504 - 511 (2007/10/02)

An enantioselective total synthesis of (+)-picrasin B (1), (+)-Δ2-picrasin B (11), and (+)-quassin (12) from the R-(-) enantiomer of the Wieland-Miescher ketone (3) employed an A-AB-ABC-ABCD sequence to assemble the tetracyclic skeleton.The cru

New quassinoid glucosides, picrasinoside-A, -B, -C, -D, -E, -F, and -G and new hemiacetals, picrasinol-A and -B, from the stem bark of Picrasma ailanthoides Planchon

Okano,Fujita,Fukamiya,Aratani

, p. 1793 - 1800 (2007/10/02)

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