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2,4,6-Trimethyl-1H-indene, a colorless to pale yellow liquid with a strong, aromatic odor, belongs to the indene family of chemicals. It is primarily utilized as a fragrance ingredient in the formulation of perfumes and colognes, and also serves as a chemical intermediate in the production of various products such as plastics, resins, and rubber. Although it is considered a low hazard chemical with no known significant health effects, it may cause irritation to the skin, eyes, and respiratory system if not handled properly, necessitating adherence to proper safety precautions during its handling and storage.

150096-40-5

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150096-40-5 Usage

Uses

Used in Fragrance Industry:
2,4,6-Trimethyl-1H-indene is used as a fragrance ingredient for its strong, aromatic odor, contributing to the unique scents of perfumes and colognes.
Used in Chemical Production:
2,4,6-Trimethyl-1H-indene is used as a chemical intermediate in the production of various products, including plastics, resins, and rubber, due to its chemical properties that facilitate the synthesis of these materials.

Check Digit Verification of cas no

The CAS Registry Mumber 150096-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,0,9 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150096-40:
(8*1)+(7*5)+(6*0)+(5*0)+(4*9)+(3*6)+(2*4)+(1*0)=105
105 % 10 = 5
So 150096-40-5 is a valid CAS Registry Number.

150096-40-5SDS

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 2,4,6-Trimethyl-1H-indene

1.2 Other means of identification

Product number -
Other names 1H-Indene,2,4,6-trimethyl

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:150096-40-5 SDS

150096-40-5Downstream Products

150096-40-5Relevant articles and documents

A bridge linking and its application of metal complexes

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Paragraph 0076, (2017/02/23)

The invention discloses a bridged metallocene complex, which is characterized by having a structural formula shown as the following A1, A2, A3 or A4. The invention also discloses a preparation method of ethylene propylene rubber. The ethylene propylene ru

A method of preparation of ethylene-propylene-diene rubber

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Paragraph 0050; 0072; 0078, (2017/03/23)

The invention discloses a bridged metallocene complex, which is characterized by having a structural formula shown as the following A1, A2, A3 or A4. The invention also discloses a preparation method of ethylene propylene rubber. The ethylene propylene ru

Synthesis and molecular structures of zirconium and hafnium complexes bearing dimethylsilandiyl-bis-2,4,6-trimethylindenyl and dimethylsilandiyl-bis- 2-methyl-4,6-diisopropylindenyl ligands

Izmer, Vyacheslav V.,Sorokin, Denis A.,Kuz'Mina, Lyudmila G.,Churakov, Andrei V.,Howard, Judith A.K.,Voskoboynikov, Alexander Z.

, p. 1067 - 1079 (2007/10/03)

Zirconium and hafnium ansa-complexes containing 2,4,6-trialkyl-substituted indenyl fragments were synthesized and unambiguously characterized. Mixtures of rac- and meso-Me2Si(2-Me-4,6-R2C9H 3-η5)2MCl2, where R = Me, i-Pr and M = Zr, Hf, were obtained by a treatment of MCl4 by dilithium salts of the respective bis(2,4,6-trialkylindenyl)dimethylsilanes in toluene. Alternatively, better yields of the same complexes can be obtained by the reaction between metal tetrachlorides and indenyl-tin derivatives gave the desired ansa-metallocenes. All rac- and meso-complexes of Zr and Hf were isolated in an analytically pure form, and six of these ansa-metallocenes were characterized by X-ray crystal structure analysis.

Process for preparing 1-indanones

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, (2008/06/13)

The present invention relates to a process for preparing 1-indanones of formula I: and isomers thereof, wherein R1, R2, R3, R4, R5, and R6 independently represent H or a C1-C20 hydrocarbon group or R1 and R2 or R2 and R3 or R3 and R4 and/or R5 and R6 together with the carbon atoms to which they are attached form a saturated or unsaturated 5- or 6-membered ring, said hydrocarbon group and/or said ring optionally containing one or more hetero atoms, said ring optionally being substituted with a C1-C4 hydrocarbon group, said process comprising reacting a compound of formula II: wherein R1, R2, R3, R4, R5, and R6 have the same meaning as defined above, with a chlorinating agent, followed by reaction with a Friedel-Crafts catalyst. The invention further relates to the preparation of the corresponding indenes.

Process for the preparation of substituted indenes and their use as ligand systems for metallocene catalysts

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, (2008/06/13)

The invention relates to a process for the preparation of a compound of the formula IV or IVa STR1 in which R1 -R5 are preferably hydrogen or alkyl, which comprises reacting a compound I STR2 with a compound II STR3 in which X1 and X2 are preferably halogen, to give the corresponding indanones, which are converted into the compounds IV and IVa by reduction and dehydration. The compounds IV and IVa are important intermediate products for the preparation of chiral metallocene complexes which are suitable catalyst components for olefin polymerization.

Process for the preparation of amorphous polymers of propylene

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, (2008/06/13)

It is possible to prepare substantially amorphous polymers of propylene endowed with high molecular weights, operating at temperatures of industrial interest, by carrying out the polymerization reaction of propylene in the presence of metallocene catalysts comprising particular bis-indenyl or bis-4,5,6,7-tetrahydroindenyl compounds substituted in the 2-position on the indenyl or tetrahydroindenyl groups.

Process for the preparation of a high molecular weight olefin polymer

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, (2008/06/13)

A very active catalyst system for olefin polymerization comprises a cocatalyst, preferably an aluminoxane, and a metallocene of the formula I STR1 in which, preferably, M1 is Zr or Hf, R1 and R2 are alkyl or halogen, R3 is hydrogen, R4 to R6 and alkyl or aryl, --(CR8 R9)m --R7 --(CR8 R9)n is a single- or multi-membered chain, in which R' can also be a (substituted) hetero atom, and m+n is zero or 1.

Process for preparing cyclopentadienyl group-containing silicon compound or cyclopentadienyl group-containing germanium compound

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, (2008/06/13)

Disclosed is a process for preparing a cyclopentadienyl group-containing silicon compound or a cyclopentadienyl group-containing germanium compound, comprising reacting (i) a lithium, sodium or potassium salt of a cyclopentadiene derivative with (ii) a silicon halide compound or a germanium halide compound in the presence of a cyanide or a thiocyanate. The cyanide or the thiocyanate is preferably a copper salt. According to the process of the invention, a cyclopentadienyl group-containing silicon compound or a cyclopentadienyl group-containing germanium compound, which is very useful for the preparation of a metallocene complex catalyst component, can be prepared in a high yield for a short period of time.

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