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3a,4,7,7a-Tetrahydro-5-methyl-1H-indene is a chemical compound belonging to the class of organic compounds, specifically indenes. It is a cyclic hydrocarbon with a molecular formula of C11H14 and a molecular weight of 146.23 g/mol. The structure of 3a,4,7,7a-Tetrahydro-5-methyl-1H-indene consists of a seven-membered ring with a methyl group attached to the 5th carbon atom and four hydrogen atoms added to the 3a, 4, 7, and 7a positions. 3a,4,7,7a-Tetrahydro-5-methyl-1H-indene is known for its aromatic properties and can be found in various natural products, such as essential oils and plant extracts. Due to its unique structure and properties, 3a,4,7,7a-tetrahydro-5-methyl-1H-indene has potential applications in the synthesis of pharmaceuticals, fragrances, and other chemical products.

7395-89-3

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7395-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7395-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7395-89:
(6*7)+(5*3)+(4*9)+(3*5)+(2*8)+(1*9)=133
133 % 10 = 3
So 7395-89-3 is a valid CAS Registry Number.

7395-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3a,4,7,7a-tetrahydro-1H-indene

1.2 Other means of identification

Product number -
Other names Indene,5-methyl-3a,4,7,7a-tetrahydro

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:7395-89-3 SDS

7395-89-3Downstream Products

7395-89-3Relevant academic research and scientific papers

PROCESS FOR PRODUCING HIGH PURITY EXO-ALKENYLNORBORNENE

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Page/Page column 17-20, (2009/07/02)

Embodiments of the present invention are directed generally to methods for producing high purity exo-alkenylnorbornenes from a mixture of conformational isomers thereof.

NEW POSSIBILITIES FOR CONTROL OF THE TRANSANNULAR CYCLIZATION OF 1,5-DIENES IN THE RITTER REACTION AS ILLUSTRATED BY METHYL-CIS-BICYCLONONA-3,7-DIENES

Nigmatova, V. B.,Andreev, V. A.,Pekhk, T. I.,Belikova, N. A.,Bobyleva, A. A.,et al.

, p. 2213 - 2223 (2007/10/02)

In the Ritter reaction 3-methyl and 3,4-dimethyl-cis-bicyclonona-3,7-dienes are converted either exclusively into acetylamines having the initial structure or into transannular cyclization products of the tricyclo3,7>nonane (brex

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