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101489-26-3

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101489-26-3 Usage

General Description

5H-Furo[3',2':4,5]furo[3,2-b]xanthen-5-one,2,3,3a,12a-tetrahydro-4,6-dihydroxy-, (3aS-cis)- (9CI) is a chemical compound that belongs to the xanthen-5-one family, which is commonly used in the synthesis of dyes and fluorescent compounds. It is a tetrahydro derivative containing four hydroxy groups on its structure, and its 3aS-cis stereochemistry contributes to its unique properties. 5H-Furo[3',2':4,5]furo[3,2-b]xanthen-5-one,2,3,3a,12a-tetrahydro-4,6-dihydroxy-, (3aS-cis)- (9CI) has potential applications in various industries, including pharmaceuticals, as well as in research and development of novel materials. Its structural and chemical properties make it a valuable building block for the creation of new compounds with diverse functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 101489-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,8 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101489-26:
(8*1)+(7*0)+(6*1)+(5*4)+(4*8)+(3*9)+(2*2)+(1*6)=103
103 % 10 = 3
So 101489-26-3 is a valid CAS Registry Number.

101489-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Dihydrosterigmatin

1.2 Other means of identification

Product number -
Other names 4,6-dihydroxy-2,3,3a,12a-tetrahydrofuro[2,3-b]furoxanth-5-one

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:101489-26-3 SDS

101489-26-3Downstream Products

101489-26-3Relevant articles and documents

Ordering the reductive and cytochrome P450 oxidative steps in demethylsterigmatocystin formation yields general insights into the biosynthesis of aflatoxin and related fungal metabolites

Henry, Kevin M.,Townsend, Craig A.

, p. 3724 - 3733 (2005)

The biosynthesis of the potent environmental carcinogen aflatoxin B1 involves ca. 15 steps beyond the first polyketide intermediate. Central among these is the rearrangement of the anthraqinone versicolorin A to the xanthone demethylsterigmatocystin. Gene

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