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1H-Indene, 2,3-dihydro-4,7-dimethyl, also known as 1H-INDENE,2,3-DIHYDRO-4,7-DIM, is a chemical compound characterized by its molecular formula C11H14. It is a colorless to pale yellow liquid with a molecular weight of 146.23 g/mol. The presence of two methyl groups on the 4 and 7 positions of the indene ring endows 1H-INDENE,2,3-DIHYDRO-4,7-DIM with unique chemical properties and reactivity, making it valuable for a range of industrial applications.

6682-71-9

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6682-71-9 Usage

Uses

Used in Pharmaceutical Industry:
1H-INDENE,2,3-DIHYDRO-4,7-DIM is used as an intermediate in the manufacture of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 1H-INDENE,2,3-DIHYDRO-4,7-DIM serves as an intermediate for the production of various agrochemicals. Its reactivity and chemical properties make it suitable for use in the synthesis of pesticides, herbicides, and other agricultural chemicals that are essential for maintaining crop health and productivity.
Used in Dye Industry:
1H-INDENE,2,3-DIHYDRO-4,7-DIM is also utilized as an intermediate in the dye industry. Its chemical properties allow it to be a part of the production process for a variety of dyes used in textiles, plastics, and other materials, adding color and vibrancy to a range of products.
Used as a Solvent in Chemical Reactions:
Due to its liquid state and chemical properties, 1H-INDENE,2,3-DIHYDRO-4,7-DIM can be used as a solvent in various chemical reactions. Its ability to dissolve other substances and facilitate reactions makes it a useful component in the chemical processing industry.
Used as a Fragrance Ingredient in Perfumes and Cosmetics:
1H-INDENE,2,3-DIHYDRO-4,7-DIM's unique chemical structure also lends itself to the creation of fragrances, making 1H-INDENE,2,3-DIHYDRO-4,7-DIM a valuable ingredient in the perfumery and cosmetics industries. It contributes to the development of scents and fragrances used in a variety of personal care products.
It is important to handle 1H-INDENE,2,3-DIHYDRO-4,7-DIM with care, as it may pose health and environmental hazards if not properly managed. Proper safety measures and disposal methods should be adhered to in order to minimize any potential risks associated with 1H-INDENE,2,3-DIHYDRO-4,7-DIM.

Check Digit Verification of cas no

The CAS Registry Mumber 6682-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,8 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6682-71:
(6*6)+(5*6)+(4*8)+(3*2)+(2*7)+(1*1)=119
119 % 10 = 9
So 6682-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14/c1-8-6-7-9(2)11-5-3-4-10(8)11/h6-7H,3-5H2,1-2H3

6682-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-dimethyl-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 4,7-DIMETHYLINDAN

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:6682-71-9 SDS

6682-71-9Relevant academic research and scientific papers

Electron Paramagnetic Resonance Spectra of the Radical Cations of Some Benzocyclobutenes, Benzocyclopentenes and Benzocyclohexenes

Avila, David V.,Davies, Alwyn G.,Li, Elizabeth R.,Ng, Kai M.

, p. 355 - 362 (2007/10/02)

1,2,4,5-Tetrahydrobenzodicyclobutene, 1,2,3,5,6,7-hexahydrobenzodicyclopentene and 1,2,3,4,6,7,8,9-octahydrobenzodicyclohexene, and their dimethyl derivatives, and tetramethylbenzocyclo-butene, -pentene and -hexene have been prepared.All except the first compound have been oxidised to their corresponding radical cations, and the EPR spectra have been analysed by assigning McConnell-type Q-values to the substituents in the benzene ring.It is suggested that the ordering of the orbital energy levels (ΨA above ΨS) in 3,6-dimethylbenzobiscyclobutene and -pentene is a manifestation of the Mills-Nixon effect, and results from rehybridisation of the strained molecular framework.In the radical cations of 5,10-dimethyl-1,2,3,4,6,7,8,9-octahydrobenzodicyclohexene and 5,6,7,8-tetramethyl-1,2,3,4-tetrahydrobenzocyclohexene the total unpaired electron density, as implied by the McConnell type of relationship, appears to be less than unity.Various possible causes of this are examined.

Compounds and compositions

-

, (2008/06/13)

The invention concerns novel compounds of the formula I STR1 wherein: W are selected from alkyl, alkenyl and alkynyl; X are selected from halogen, nitro, cyano, alkyl, substituted alkyl, hydroxy, alkoxy, substituted alkoxy, alkenyl, alkynyl, alkenyloxy, alkynyloxy, acyloxy, alkoxycarbonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, sulfamoyl, substituted sulfamoyl, amino, substituted amino, and the groups formyl and alkanoyl and the oxime and imine derivatives thereof, and an alkylene group which bridges two adjacent carbon atoms of the benzene ring; R1 is selected from hydrogen, alkyl, alkenyl, alkynyl, substituted alkyl, alkylsulfonyl, arylsulfonyl, acyl and an inorganic or organic cation; R2 is selected from alkyl, substituted alkyl, alkenyl, haloalkenyl, alkynyl and haloalkynyl; R3 is selected from alkyl, fluoroalkyl, alkenyl, alkynyl, and phenyl; p is zero or an integer selected form 1 to 4; n is zero or an integer selected from 1 to 3; and m is zero or an integer selected from 1 to 3. The compounds of the invention show cereal selective herbicidal properties and plant growth regulating properties and in further embodiments the invention provides processes for the preparation of the compounds of formula I, intermediates useful in the preparation of the compounds of formula I, compositions containing as active ingredient a compound of formula I, and herbicidal and plant growth regulating processes utilizing compounds of formula I.

FACILE SYNTHESIS OF (3aS)-1,3a-DIMETHYL-2,3,3a,5,6,7-HEXAHYDROINDEN-4(5H)-ONE, AN INTERMEDIATE FOR STEROID SYNTHESIS

Jung, Michael E.,Hatfield, Gregory L.

, p. 3175 - 3178 (2007/10/02)

The optically active Wieland-Miescher ketone 2 has been converted in six steps to the enone 9, a potentially useful synthon for optically active steroid and terpene synthesis.

NOVEL OXIDATIVE REARRANGEMENT OF β,γ-UNSATURATED KETONE HYDRAZONES ON IODINATION IN BASE

Jung, Michael E.,Hatfield, Gregory L.

, p. 3991 - 3994 (2007/10/02)

Iodination of the bicyclic enone hydrazone 3 in excess triethylamine gave, in addition to the expected vinyl iodide 4, the rearranged aromatic product 5.

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