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88182-33-6

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  • 1H-5,10c-Ethanonaphtho[1,2-c:7,8-c']difuran- 3,10-dione,1,8-dibutylidene-5,5a,6,7,8,10bhexahydro-,(1Z,5S,5aS,8Z,10bS,10cS)- 88182-33-6

    Cas No: 88182-33-6

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88182-33-6 Usage

General Description

Levistilide A is a natural chemical compound found in the roots of a traditional Chinese medicinal plant called Ligusticum chuanxiong. It belongs to the class of phthalides and has been identified as an active ingredient responsible for the plant's pharmacological effects. Levistilide A has been studied for its potential therapeutic properties, including anti-inflammatory, neuroprotective, and cardiovascular protective activities. It has shown promising results in various preclinical studies, demonstrating its potential as a drug candidate for the treatment of neurological and cardiovascular diseases. Further research is needed to fully understand the pharmacological effects and potential applications of Levistilide A.

Check Digit Verification of cas no

The CAS Registry Mumber 88182-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,8 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88182-33:
(7*8)+(6*8)+(5*1)+(4*8)+(3*2)+(2*3)+(1*3)=156
156 % 10 = 6
So 88182-33-6 is a valid CAS Registry Number.

88182-33-6SDS

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 levistolide A

1.2 Other means of identification

Product number -
Other names diligustilide

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:88182-33-6 SDS

88182-33-6Upstream product

88182-33-6Downstream Products

88182-33-6Relevant articles and documents

Chemical reactivity of phthalides. Relay synthesis of diligustilide, rel-(3'R)-3',8'-dihydrodiligustilide and wallichilide

Rios, Maria Yolanda,Delgado, Guillermo,Toscane, Ruben A.

, p. 3355 - 3366 (2007/10/03)

Diels Alder reaction using Z-ligustilide (3) both as diene and dienophile afforded the natural product diligustilide (1). The relay synthesis of 5 from 1 (via situ-selective lactone ring opening, reduction with NaBH4/MeOH and lactonization with SOCl2/THF) was achieved and confirmed the revised structure of 5, a secondary constituent of Ligusticum wallichii. The natural substance wallichilide (8) was also obtained directly from 1.

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