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1H-3b,8-(Epoxyethano)cyclopent[a]inden-10-one,3a,4,5,6,7,7a,8,8a-octahydro-3a,4,7a,8a-tetrahydroxy-2-(2-hydroxy-1-methylethyl)-3,5,8-trimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75765-19-4

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75765-19-4 Usage

Chemical class

Cyclopent[a]indenone derivative

Octahydro

Eight hydrogen atoms are present in the compound's structure.

Tetrahydroxy

Four hydroxyl (-OH) groups are present in the compound.

Trisubstituted

Three methyl groups are present in the compound.

Isopropyl substituent

A 2-hydroxy-1-methylethyl (isopropyl) group is present in the compound.

Epoxyethano

An epoxy group connected to an ethano (two-carbon) chain.

Hydroxyl groups

Four hydroxyl groups are present, contributing to the compound's polarity and potential reactivity.

Pharmaceuticals

Due to its complex structure and multiple functional groups, the compound may have unique biological activities that could be useful in drug development.

Cosmetics

The compound's hydroxyl groups may provide potential benefits in the formulation of cosmetic products, such as moisturizing or antioxidant properties.

Research

The compound's intricate structure and potential biological activities make it an interesting candidate for further exploration and research in various fields.

Molecular weight

Approximately 346.4 g/mol (calculated from the molecular formula)

Stereochemistry

The compound may have stereocenters (chiral centers) due to the presence of multiple hydroxyl and methyl groups. This could result in different stereoisomers with potentially different properties and activities.

Solubility

The compound's hydroxyl groups may make it soluble in polar solvents, such as water or alcohols, while its non-polar methyl groups may also provide some solubility in non-polar solvents, such as hexane or chloroform.

Stability

The presence of multiple hydroxyl groups and an epoxyethano group may make the compound sensitive to certain conditions, such as heat, light, or acidic/basic environments. Careful handling and storage may be required to maintain the compound's stability.

Check Digit Verification of cas no

The CAS Registry Mumber 75765-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,6 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75765-19:
(7*7)+(6*5)+(5*7)+(4*6)+(3*5)+(2*1)+(1*9)=164
164 % 10 = 4
So 75765-19-4 is a valid CAS Registry Number.

75765-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Cinncassiol A

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:75765-19-4 SDS

75765-19-4Relevant academic research and scientific papers

The Constituents of Cinnamomi Cortex. I. Structures of Cinncassiol A and Its Glucoside

Yagi, Akira,Tokubuchi, Nobutaka,Nohara, Toshihiro,Nonaka, Genichiro,Nishioka, Itsuo,Koda, Akihide

, p. 1432 - 1436 (2007/10/02)

Compounds I-X were isolated from the water extractive of Cinnamomi Cortex, which shows anti-complement activity.Among them, the structures of I-VI were clarified on the basis of chemical and spectral studies.Compounds I and II were identified as cinnzeylanine and cinnzeylanol, respectively.Compounds III and IV were proved to be dehydrated products of I and II, respectively.Compound V was shown to be 19-hydroxylated IV and was named cinncassiol A.VI was identified as cinncassiol A 19-O-β-D-glucopyranoside.Keywords - Cinnamomi Cortex; diterpenoids; anti-complement activity; cinncassiol A; cinncassiol A 19-O-β-D-glucopyranoside

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