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1H-4b,12-Ethenochrysene-7-carboxylicacid,4,4a,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-7,10a-dimethyl-13-(1-methylethyl)-1,4-dioxo-,(4aR,4bS,6aR,7R,10aR,10bR,12R,12aR)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22422-38-4

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22422-38-4 Usage

Molecular Structure

A complex polycyclic aromatic hydrocarbon derived from chrysene.

Explanation

The compound is based on a chrysene structure, which consists of four fused benzene rings.

Explanation

The presence of the carboxylic acid group (-COOH) at the 7-position of the chrysene core contributes to its chemical reactivity and properties.

Explanation

The compound has 14 hydrogen atoms added to the core structure, making it a saturated hydrocarbon.

Explanation

Two methyl groups (-CH3) are attached to the 10a position of the molecule, which can influence its steric and electronic properties.

Explanation

An isopropyl group (-CH(CH3)2) is attached to the 13-position, further affecting the compound's properties and reactivity.

Explanation

The core structure of the compound consists of a 13-membered ring, which is relatively uncommon in organic compounds and can influence its properties and reactivity.

Explanation

The compound has specific three-dimensional arrangements of its atoms, which can affect its properties, reactivity, and potential applications.

Explanation

Due to its complex structure and various functional groups, the compound may have applications in the synthesis of other compounds, drug development, or as a component in material science.

Explanation

The complex nature of the compound requires further investigation to fully understand its properties, reactivity, and potential applications in various fields.

Carboxylic Acid Group

Contains a 7-carboxylic acid group.

Tetradecahydro

Saturated with 14 hydrogen atoms.

Dimethyl Substituent

Has a 10a-dimethyl group.

Isopropyl Substituent

Contains a 13-(1-methylethyl) group.

13-Membered Ring Structure

The compound features a 13-membered ring.

Stereochemical Configurations

The compound has various stereochemical configurations denoted by R and S designations.

Applications

Potential uses in organic synthesis, pharmaceuticals, or material science.

Further Research

Properties and potential uses need to be explored through laboratory research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 22422-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22422-38:
(7*2)+(6*2)+(5*4)+(4*2)+(3*2)+(2*3)+(1*8)=74
74 % 10 = 4
So 22422-38-4 is a valid CAS Registry Number.

22422-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name quinopimaric acid

1.2 Other means of identification

Product number -
Other names (4aR)-1.4-Dioxo-7t.10at-dimethyl-13-isopropyl-(4arH.6acH.10bcH.12acH)-Δ2-tetradecahydro-4aH-4bt.12t-aetheno-chrysen-carbonsaeure-(7c)

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:22422-38-4 SDS

22422-38-4Upstream product

22422-38-4Downstream Products

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