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1,3,5-Cycloheptatriene,1-methoxy-4-(1-methylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126893-59-2

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126893-59-2 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms, 16 hydrogen (H) atoms, and 1 oxygen (O) atom.

Explanation

The compound is derived from cycloheptatriene, which is a seven-membered ring with three carbon-carbon double bonds. It has a methoxy (-OCH3) group and an isopropyl (-CH(CH3)2) group attached to the molecule.

Explanation

The name follows the IUPAC nomenclature rules, indicating the positions of the methoxy and isopropyl groups on the cycloheptatriene ring.

Explanation

The compound is used as a reagent in various organic reactions, making it valuable in the fields of chemical research, pharmaceuticals, and agrochemicals.

Explanation

Due to its unique structure and properties, the compound has potential applications in a wide range of scientific and industrial processes.

Explanation

The material does not provide information about the physical properties of the compound, such as melting point, boiling point, density, or solubility.

Explanation

The material does not provide information about the chemical properties of the compound, such as reactivity, stability, or specific reactions it undergoes.

Explanation

The material does not provide information about the safety precautions or handling procedures for the compound. It is essential to follow proper safety protocols when working with chemicals, especially in a laboratory setting.

Structure

Cycloheptatriene derivative with a methoxy group and an isopropyl group

Applications

Organic synthesis, chemical research, pharmaceutical, and agrochemical industries

Potential Uses

Scientific and industrial purposes

Physical Properties

Not provided in the material

Chemical Properties

Not provided in the material

Safety and Handling

Not provided in the material

Check Digit Verification of cas no

The CAS Registry Mumber 126893-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126893-59:
(8*1)+(7*2)+(6*6)+(5*8)+(4*9)+(3*3)+(2*5)+(1*9)=162
162 % 10 = 2
So 126893-59-2 is a valid CAS Registry Number.

126893-59-2SDS

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-Isopropyl-1-methoxy-cyclohepta-1,3,5-triene

1.2 Other means of identification

Product number -
Other names -

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:126893-59-2 SDS

126893-59-2Downstream Products

126893-59-2Relevant academic research and scientific papers

Anodic oxidation of cycloheptatriene systems and its application to the synthesis of non-benzenoid aromatic compounds

Shono, Tatsuya,Nozoe, Tetsuo,Maekawa, Hirofumi,Yamaguchi, Yoshihide,Kanetaka, Shinya,Masuda, Haruhisa,Okada, Toshio,Kashimura, Shigenori

, p. 593 - 603 (2007/10/02)

Anodic oxidation of cycloheptatrienes has been found to be one of the most powerful key tools for the preparation of a variety of non-benzenoid aromatic compounds such as tropylium salts, tropones, tropolones, 2H-cyclohepta[b]furan-2-ones, and azulenes.

A NOVEL REGIOSELECTIVE SYNTHESIS OF 4-SUBSTITUTED TROPONES

Shono, Tatsuya,Naekawa, Hirofumi,Nozoe, Tetsuo,Kashimura, Shigenori

, p. 895 - 898 (2007/10/02)

The preparation of 4-alkyl (or aryl) tropones has easily been accomplished by the anodic oxidation of 1-methoxy-4-alkyl (or aryl) cycloheptatrienes which where synthesized by the regioselective addition of alkyl or aryl lithium to 3-position of 7,7-dimethoxycycloheptatriene followed by the thermal 1,5-hydrogen shift of the resulting 3-methoxy-7-alkyl (or aryl) cycloheptatrienes.

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