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Homopterocarpin is a phytoalexin, a type of plant antibiotic, found predominantly in legumes such as soybeans and peanuts. It is a member of the pterocarpans group, which are recognized for their antimicrobial and anti-fungal characteristics. Homopterocarpin is synthesized by plants as a defense mechanism against pathogen attacks or stress, and it has been suggested to possess antioxidant and anti-inflammatory properties. These attributes make homopterocarpin a compound of interest for potential applications in pharmaceuticals and agriculture, as well as in enhancing plant resistance to diseases and stress.

606-91-7

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606-91-7 Usage

Uses

Used in Pharmaceutical Applications:
Homopterocarpin is used as an antimicrobial and anti-fungal agent for its natural defense properties against invading pathogens. Its potential antioxidant and anti-inflammatory properties further position it as a candidate for developing new pharmaceuticals aimed at treating various diseases and conditions.
Used in Agricultural Applications:
In agriculture, homopterocarpin is utilized to enhance plant resistance to diseases and stress. By leveraging its natural defense mechanisms, it can potentially improve crop health and reduce the need for chemical interventions, contributing to more sustainable farming practices.
Used in Plant Disease Resistance:
Homopterocarpin is employed to bolster a plant's inherent resistance to diseases. Its role in the plant's defense system can be harnessed to develop strategies for protecting crops from a range of pathogens, thereby increasing yield and reducing losses due to disease.

Check Digit Verification of cas no

The CAS Registry Mumber 606-91-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 606-91:
(5*6)+(4*0)+(3*6)+(2*9)+(1*1)=67
67 % 10 = 7
So 606-91-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O4/c1-18-10-4-6-13-15(7-10)20-9-14-12-5-3-11(19-2)8-16(12)21-17(13)14/h3-8,14,17H,9H2,1-2H3/t14-,17-/m0/s1

606-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Homopterocarpin

1.2 Other means of identification

Product number -
Other names 6H-Benzofuro[3,2-c][1]benzopyran, 6a,11a-dihydro-3,9-dimethoxy-, (6aR-cis)-

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:606-91-7 SDS

606-91-7Downstream Products

606-91-7Relevant academic research and scientific papers

A new regioselective synthesis of pterocarpans

Engler, Thomas A.,Combrink, Keith D.,Reddy, Jayachandra P.

, p. 454 - 455 (2007/10/02)

Pterocarpans are formed directly and efficiently via titanium(IV) catalysed reactions of 2H-chromenes and 2-alkoxy-1,4-benzoquinones.

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