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Cleroindicin D, a natural chemical compound derived from the plants of the genus Clerodendrum, is a member of the diterpenoid class. It exhibits a range of pharmacological activities, such as anti-inflammatory, antioxidant, and antitumor properties. Additionally, it has demonstrated potential in the prevention of neurodegenerative diseases and as an antibacterial agent. With its diverse biological activities, Cleroindicin D is a significant molecule in the pursuit of new pharmaceuticals and a promising candidate for the development of drugs targeting a variety of conditions.

189264-45-7

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189264-45-7 Usage

Uses

Used in Pharmaceutical Industry:
Cleroindicin D is used as a pharmaceutical candidate for its anti-inflammatory properties, making it suitable for the treatment of inflammatory conditions.
Cleroindicin D is used as a pharmaceutical candidate for its antioxidant properties, which can help in the prevention of oxidative stress-related diseases.
Used in Anticancer Applications:
Cleroindicin D is used as an anticancer agent, potentially effective against various types of cancer due to its antitumor properties.
Used in Neuroprotection:
Cleroindicin D is used as a neuroprotective agent for its potential in preventing neurodegenerative diseases.
Used in Antibacterial Applications:
Cleroindicin D is used as an antibacterial agent, effective against certain types of bacteria, contributing to the development of new antimicrobial drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 189264-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,2,6 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 189264-45:
(8*1)+(7*8)+(6*9)+(5*2)+(4*6)+(3*4)+(2*4)+(1*5)=177
177 % 10 = 7
So 189264-45-7 is a valid CAS Registry Number.

189264-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aR,4R,7aR)-3a,4-Dihydroxyhexahydro-1-benzofuran-6(2H)-one

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:189264-45-7 SDS

189264-45-7Relevant academic research and scientific papers

Desymmetrization of cyclohexadienones via bronsted acid-catalyzed enantioselective oxo-michael reaction

Gu, Qing,Rong, Zi-Qiang,Zheng, Chao,You, Shu-Li

supporting information; experimental part, p. 4056 - 4057 (2010/05/01)

Chemical Reaction Reprentation Desymmetrlzatlon of cyclohexadlenones via enantloselectlve oxo-Mlchael reaction catalyzed by chlral phosphoric add to afford highly enantloenrlched 1,4-dloxane and tetrahydrofuran derivatives In excellent yields has been realized. The newly established methodology allows the facile enantloselectlve synthesis of clerolndlclns C, D, and F.Copyright

Catalytic enantioselective silylation of acyclic and cyclic triols: Application to total syntheses of cleroindicins D, F, and C

You, Zhen,Hoveyda, Amir H.,Snapper, Marc L.

supporting information; experimental part, p. 547 - 550 (2009/04/14)

(Chemical Equation Presented) Pick one out of three: Acyclic and cyclic 1,2,3-triols are silylated with exceptional site- and enantioselectivity by a small-molecule catalyst to afford silyl ethers having a neighboring diol moiety. The new process is appli

Enantioselective total synthesis of all of the known chiral cleroindicins (C-F): Clarification among optical rotations and assignments

Wenderski, Todd A.,Huang, Shenlin,Pettus, Thomas R. R.

supporting information; experimental part, p. 4104 - 4109 (2009/09/25)

(Chemical Equation Presented) Enantioselective syntheses of all of the named chiral members of the cleroindicin family (C-F) are reported. This effort demonstrates the synthetic utility of a 2,4-dihydroxybenzaldehyde as a starting material for natural pro

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