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Atractylodinol is a natural compound derived from the rhizomes of Atractylodes lancea, a plant commonly used in traditional medicine. It possesses antimicrobial properties and has been identified as a potent inhibitor of the porcine reproductive and respiratory syndrome virus (PRRSV).

61642-89-5

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61642-89-5 Usage

Uses

Used in Antimicrobial Applications:
Atractylodinol is used as an antimicrobial agent for its differential antimicrobial activity, which can be effective against various pathogens.
Used in Veterinary Medicine:
In the veterinary industry, Atractylodinol is used as an antiviral agent for the inhibition of PRRSV, a virus that causes significant economic losses in the pig farming industry. Its use can help in controlling the spread of the virus and improving the health of the animals.
Used in Drug Development:
Atractylodinol's potent inhibitory effects on PRRSV make it a promising candidate for the development of new antiviral drugs, particularly for the treatment of porcine reproductive and respiratory syndrome.

Check Digit Verification of cas no

The CAS Registry Mumber 61642-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,4 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61642-89:
(7*6)+(6*1)+(5*6)+(4*4)+(3*2)+(2*8)+(1*9)=125
125 % 10 = 5
So 61642-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O2/c14-11-7-5-3-1-2-4-6-9-13-10-8-12-15-13/h5-10,12,14H,11H2/b7-5+,9-6+

61642-89-5SDS

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 (2E,8E)-9-(Furan-2-yl)nona-2,8-dien-4,6-diyn-1-ol

1.2 Other means of identification

Product number -
Other names (2E,8E)-9-(furan-2-yl)nona-2,8-dien-4,6-diyn-1-ol

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:61642-89-5 SDS

61642-89-5Downstream Products

61642-89-5Relevant academic research and scientific papers

A direct synthesis of atractylodinol, a potent inhibitor of PRRSV, and its biological evaluation

Kraus, George A.,Dong, Pengfei,Qu, Yang,Evans, Alyssa,Carpenter, Susan

, p. 5185 - 5187 (2016)

A direct synthesis of atractylodinol from 2-furylbutenyne and bromoacetylene 6 is reported. Both compounds 1 and 8 showed greater than 99% virus inhibition.

A new 9-nor-atractylodin from Atractylodes lancea and the antibacterial activity of the atractylodin derivatives

Chen, Yanjun,Wu, Yuxue,Wang, Hexiang,Gao, Kun

, p. 199 - 203 (2012)

A new compound, namely, 9-nor-atractylodin (1) and one known atractylodin (2) were isolated from the rhizomes of Atractylodes lancea. The structural modifications of atractylodin were carried out and a series of atractylodin derivatives (3-10) were obtain

Total synthesis of 1-(Z)-atractylodinol

Oliveira, Juliana M.,Zeni, Gilson,Malvestiti, Ivani,Menezes, Paulo H.

, p. 8183 - 8185 (2007/10/03)

The total synthesis of 1-(Z)-atractylodinol, a natural polyacetylenic alcohol with several biological activities, has been achieved using a newly developed telluride synthon and a novel use for the Negishi type coupling reaction employing vinyl tellurides.

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