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3,8-dimethyl-5-(propan-2-yl)-5,6,7,8-tetrahydronaphthalene-1,2-dione is a complex organic compound with a molecular formula of C15H20O2. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with four carbon atoms added to the structure, forming a tetracyclic compound. The molecule features two methyl groups at the 3rd and 8th positions, a propyl group attached to the 5th position, and a 1,2-dione functional group, which consists of two carbonyl groups (C=O) connected to the same carbon atom. 3,8-dimethyl-5-(propan-2-yl)-5,6,7,8-tetrahydronaphthalene-1,2-dione is characterized by its unique structure and properties, making it a potential candidate for various chemical and pharmaceutical applications.

7715-94-8

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7715-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7715-94-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7715-94:
(6*7)+(5*7)+(4*1)+(3*5)+(2*9)+(1*4)=118
118 % 10 = 8
So 7715-94-8 is a valid CAS Registry Number.

7715-94-8SDS

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 3,8-dimethyl-5-propan-2-yl-5,6,7,8-tetrahydronaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 5,6,7,8-tetrahydro-3,8-dimethyl-5-isopropyl-1,2-naphthoquinone

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:7715-94-8 SDS

7715-94-8Upstream product

7715-94-8Downstream Products

7715-94-8Relevant academic research and scientific papers

Iodoxybenzene Oxidation of 1-Naphthols: Synthesis of Mansonone A

Murali, D.,Krishna Rao, G. S.

, p. 668 - 670 (2007/10/02)

Substituted 1-naphthols (1a-g) have been oxidized by iodoxybenzene to afford a mixture of the corresponding 1,2-(2a-g)-and 1,4-(3a-g)-naphthoquinones.Similar oxidation of a tetrahydro-8-naphthol (8-hydroxycalamenene) (4) gives mansonone-A (5) and a 1,4-quinone (6).During oxidation iodoxybenzene preserves intact labile structural features such as a benzylic tertiary hydroxyl group or a hydroaromatic ring.

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