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13656-81-0

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13656-81-0 Usage

Description

4-Isopropyltropone is an organic compound with the molecular formula C10H16O, characterized by its unique structure and properties. It is a derivative of tropone, a seven-membered ring with a carbonyl group and a double bond, and features an isopropyl group attached to the fourth position of the ring. 4-Isopropyltropone is known for its distinct chemical and physical properties, making it a versatile molecule with potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
4-Isopropyltropone is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Synthesis:
In the field of organic chemistry, 4-Isopropyltropone serves as a valuable building block for the synthesis of more complex molecules. Its reactivity and structural features make it a useful starting material for creating a wide range of chemical products, including fragrances, dyes, and other specialty chemicals.
Used in Flavor and Fragrance Industry:
Due to its distinct aroma and volatility, 4-Isopropyltropone is used as a component in the creation of various fragrances and flavors. Its unique scent profile can be utilized to enhance or modify the overall aroma of perfumes, colognes, and other scented products.
Used in Research and Development:
4-Isopropyltropone is also employed in research and development settings, where it can be used to study the properties and behavior of similar compounds. Its unique structure and reactivity make it an interesting subject for scientific investigation, potentially leading to new discoveries and innovations in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 13656-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,5 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13656-81:
(7*1)+(6*3)+(5*6)+(4*5)+(3*6)+(2*8)+(1*1)=110
110 % 10 = 0
So 13656-81-0 is a valid CAS Registry Number.

13656-81-0SDS

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 4-isopropylcyclohepta-2,4,6-trienone

1.2 Other means of identification

Product number -
Other names hinokitiol

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:13656-81-0 SDS

13656-81-0Downstream Products

13656-81-0Relevant articles and documents

Takaya et al.

, p. 1778,1784 (1978)

Jones

, p. 1230,1232 (1970)

HINOKITIOL ANALOGUES, METHODS OF PREPARING AND PHARMACEUTICAL COMPOSITIONS THEREOF

-

Page/Page column 25; 165, (2019/11/04)

Disclosed are analogues of hinokitiol, methods for preparing them, and pharmaceutical compositions thereof. Also disclosed are methods for their use in treating iron-related diseases.

Cycloaddition of acyclic conjugated dienes with a tetrachloro- substituted oxyallyl intermediate generated from pentachloroacetone

Foehlisch, Baldur,Korfant, Hilmar,Meining, Holger,Frey, Wolfgang

, p. 1335 - 1344 (2007/10/03)

Pentachloroacetone (1) reacts with several conjugated dienes in the presence of sodium trifluoroethoxide/trifluoroethanol to form cycloadducts of a tetrachlorooxyallyl intermediate 6, mainly in the [4+3] mode. Representative [4+3] cycloadducts, i.e. α,α,α',α'- tetrachlorocycloheptenones 9, have been dehalogenated and dehydrohalogenated, furnishing α,α'-dichlorotropones 15 in high yields.

Anodic oxidation of cycloheptatriene systems and its application to the synthesis of non-benzenoid aromatic compounds

Shono, Tatsuya,Nozoe, Tetsuo,Maekawa, Hirofumi,Yamaguchi, Yoshihide,Kanetaka, Shinya,Masuda, Haruhisa,Okada, Toshio,Kashimura, Shigenori

, p. 593 - 603 (2007/10/02)

Anodic oxidation of cycloheptatrienes has been found to be one of the most powerful key tools for the preparation of a variety of non-benzenoid aromatic compounds such as tropylium salts, tropones, tropolones, 2H-cyclohepta[b]furan-2-ones, and azulenes.

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