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59901-98-3

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59901-98-3 Usage

Molecular Structure

Contains a benzene ring fused to a cyclopentene ring, with oxygen atoms at various positions.

Chemical Classification

Alcohol (indicated by the "-ol" suffix)

Applications

Utilized in organic synthesis.
Used as a building block for more complex molecules.
Potential applications in pharmaceutical and materials industries.

Specific Uses

Creation of novel drugs or materials due to its unique structure and reactivity.

Research Interest

Studied for structure-activity relationships of organic compounds.
Investigated for its role in various biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 59901-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,0 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59901-98:
(7*5)+(6*9)+(5*9)+(4*0)+(3*1)+(2*9)+(1*8)=163
163 % 10 = 3
So 59901-98-3 is a valid CAS Registry Number.

59901-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Hydroxy-8,9-methylenedioxypterocarpene

1.2 Other means of identification

Product number -
Other names -

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:59901-98-3 SDS

59901-98-3Downstream Products

59901-98-3Relevant articles and documents

METABOLISM OF THE PHYTOALEXINS MEDICARPIN AND MAACKIAIN BY FUSARIUM SOLANI

Denny, Timothy P.,Vanetten, Hans D.

, p. 1023 - 1028 (1982)

Non-inhibitory concentrations of the pterocarpan phytoalexin medicarpin were completely metabolized by isolates of Fusarium solani f.sp. pisi, f. sp. cucurbitate, f. sp. phaseoli and two other F. solani isolates genetically related to f. sp. pisi during 24 hr of growth in liquid medium.The major metabolic products accumulated without significant further degradation.Medicarpin was modified at one of three adjacent carbon atoms to form either an isoflavanone derivative, a 1a-hydroxydienone derivative or 6a-hidroxymedicarpin.Whereas each isolate degraded medicarpin to one or more metabolites, the isolates varied as to which metabolite they produced.Maackiain, another pterocarpan phytoalexin, was also metabolized by all the isolates to products analogous to those formed from medicarpin.The ability to metabolize medicarpin and maackiain was not always associated with the ability to metabolize pisatin and phaseollin, two other pterocarpan phytoalexins that were degraded by several of the isolates.Tolerance of medicarpin and maackiain was similarly not always associated with tolerance to pisatin. Key Word Index- Fusarium solani; Nectria haematococca; fungi; phytoalexin metabolism; pterocarpan; oxygenation; isoflavanone; 1a-hydroxydienone; 6a-hydroxypterocarpan.

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