Welcome to LookChem.com Sign In|Join Free
  • or
2,4,6-Cycloheptatrien-1-one, 4-methyl-, also known as methylbenzene, is a clear, colorless liquid characterized by a pungent, aromatic odor. It is a versatile organic compound that finds use in various industrial applications due to its solvent properties and chemical reactivity.
Used in Coatings Industry:
2,4,6-Cycloheptatrien-1-one, 4-methylis used as a solvent in the coatings industry for lacquers, paints, and varnishes. Its ability to dissolve a wide range of substances makes it a valuable component in these formulations, enhancing the performance and application of the final product.
Used in Dye Production:
In the dye industry, 2,4,6-Cycloheptatrien-1-one, 4-methylis utilized in the production of various dyes. Its chemical properties allow it to act as a solvent or a reactant in the synthesis of dyes, contributing to the coloration and stability of textiles and other materials.
Used in Perfumery:
2,4,6-Cycloheptatrien-1-one, 4-methylis used as a solvent and carrier in the perfumery industry. Its aromatic properties make it suitable for blending with other fragrance components, helping to create complex and long-lasting scents.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical sector, 2,4,6-Cycloheptatrien-1-one, 4-methylserves as a solvent and intermediate in the synthesis of various drugs. Its versatility in chemical reactions enables the production of a wide range of medicinal compounds.
However, it is crucial to note that 2,4,6-Cycloheptatrien-1-one, 4-methylis highly flammable and can cause irritation to the skin, eyes, and respiratory system upon contact or inhalation. Prolonged exposure may also lead to central nervous system effects and organ damage. Therefore, it is imperative to handle this chemical with caution and implement proper safety measures during its use.

1654-62-2

Post Buying Request

1654-62-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1654-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1654-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1654-62:
(6*1)+(5*6)+(4*5)+(3*4)+(2*6)+(1*2)=82
82 % 10 = 2
So 1654-62-2 is a valid CAS Registry Number.

1654-62-2SDS

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-methyltropone

1.2 Other means of identification

Product number -
Other names 4-Methyl-cycloheptatrienon

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:1654-62-2 SDS

1654-62-2Downstream Products

1654-62-2Relevant academic research and scientific papers

Reaction of atomic carbon with isomeric cresols

Soekmen, Ilkay,Ece, Abdulilah,Duez, Buelent,Sevin, Fatma

experimental part, p. 650 - 653 (2010/06/16)

Reaction of atomic carbon with isomeric cresols generates methyltropones and xylenols. Methyltropone to xylenol ratio was found to be highest for m-cresol and lowest for p-cresol. Stability of singlet carbenes produced after insertion of atomic carbon int

Photoreactions of 4-(tribromomethyl)-4-methyl-2,5-cyclohexadienone and its derivatives with amines: Radical cyclization and ring expansion reactions promoted through photoinduced electron transfer processes

Hasegawa, Eietsu,Tamura, Yukinobu,Suzuki, Kimiko,Yoneoka, Akira,Suzuki, Toshio

, p. 8780 - 8785 (2007/10/03)

Photoreactions of 4-(tribromomethyl)-4-methyl-2,5-cyclohexadienone (1) and its derivatives with amines were studied. Irradiation of 1 with amine produced 4-bromo-5-methyltropone (2) along with 4-(dibromomethyl)-4-methyl- 2,5-cyclohexadienone (3). The effects of solvent, added water, and the structural variation in amine on the product ratio were explored. Isolation of the amine-derived products revealed that oxidative dealkylation of amine proceeded during the photoreaction. On the basis of the results obtained, a reaction mechanism involving fragmentation of the dienone anion-radical and amine cation-radical pair is proposed. Photoreactions of dienone 4 with amine produced the tropones 6 and 7, whereas tropone 9 was produced from 8. Trialkyltin radical-induced reductions of dienones 1 and 4 with tri-n- butyltin hydride demonstrated common features with the photoreactions. It was also found that irradiation of dienone 3 with amine produced 4-methyltropone (10).

Reaction of 4-methyl-4-tribromomethylcyclohexa-2,5-dien-1-one with zinc metal

Gavrilova,Gavrilov,Butin

, p. 179 - 180 (2007/10/03)

4-Methyl-4-tribromomethylcyclohexa-2,5-dien-1-one reacts with zinc dust in absolute DMF to give a mixture of 4-bromo-5-methylcyclohepta-2,4,6-trien-1-one, 4-methyl-cyclohepta-2,4,6-trien-1-one, and 4-dibromomethyl-4-methylcyclohexa-2,5-dien-1-one.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1654-62-2