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TRIMETHYL 4-BROMOORTHOBENZOATE is a chemical compound characterized by the molecular formula C10H11BrO2. It is an orthobenzoic acid derivative, featuring a bromine atom at the 4-position and three methyl groups at the ortho position. TRIMETHYL 4-BROMOORTHOBENZOATE is recognized for its stability and relative non-reactivity under standard conditions, making it a valuable intermediate in various chemical syntheses.

104865-88-5

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104865-88-5 Usage

Uses

Used in Pharmaceutical Industry:
TRIMETHYL 4-BROMOORTHOBENZOATE is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, contributing to advancements in medicine.
Used in Agrochemical Industry:
In the agrochemical sector, TRIMETHYL 4-BROMOORTHOBENZOATE serves as an essential building block for the creation of agrochemicals. Its incorporation aids in the development of effective products for agricultural use, such as pesticides and herbicides, enhancing crop protection and yield.
Used in Flavors and Fragrances Industry:
TRIMETHYL 4-BROMOORTHOBENZOATE is employed as a component in the production of flavors and fragrances. Its chemical properties enable the creation of distinct scents and tastes, adding value to the final products in the perfumery, food, and beverage industries.
Used in Organic Compounds Synthesis:
TRIMETHYL 4-BROMOORTHOBENZOATE also acts as a versatile building block in the synthesis of other organic compounds. Its reactivity and structural features make it suitable for use in organic chemistry, facilitating the production of a wide range of chemical products for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 104865-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104865-88:
(8*1)+(7*0)+(6*4)+(5*8)+(4*6)+(3*5)+(2*8)+(1*8)=135
135 % 10 = 5
So 104865-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BrO3/c1-12-10(13-2,14-3)8-4-6-9(11)7-5-8/h4-7H,1-3H3

104865-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-(trimethoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names Trimethyl 4-bromoorthobenzoate

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:104865-88-5 SDS

104865-88-5Relevant academic research and scientific papers

Anodic oxidation of dithiane carboxylic acids: A rapid and mild way to access functionalized orthoesters

Denis, Camille,Dobbs, Adrian P.,Garcia, Anthony D.,Goodall, Iain C. A.,Lam, Kevin,Leech, Matthew C.,Petti, Alessia

, p. 4000 - 4005 (2020/06/08)

A new electrochemical methodology has been developed for the preparation of a wide variety of functionalized orthoesters under mild and green conditions from easily accessible dithiane derivatives. The new methodology also offers an unprecedented way to access tri(fluorinated) orthoesters, a class of compound that has never been studied before. This provides the community with a rapid and general method to prepare libraries of functionalized orthoesters from simple and readily available starting materials.

INDIRECT ELECTROCHEMICAL SIDE-CHAIN OXIDATION OF ALKYL AROMATIC COMPOUNDS - SELECTIVE SYNTHESIS OF METHYL BENZOATES OR ORTHOBENZOIC ACID TRIMETHYLESTERS

Brinkhaus, Karl-Heinz Grosse,Steckhan, Eberhard,Degner, Dieter

, p. 553 - 560 (2007/10/02)

The technically important side-chain oxidation of alkyl aromatic compounds to form either methyl benzoates or orthobenzoic acid trimethylesters can be performed electrochemically at low potentials in methanol solution using an undivided cell and tris(2,4-dibromophenyl)amine as redox catalyst.Under neutral or slightly acidic conditions methyl benzoates are selectively formed while under basic conditions the orthoesters are predominating.In a similar way ortho benzoic acid trimethylesters are formed selectively starting from benzaldehyde dimethylacetals.The redox catalyst is stable under the reaction conditions so that several thousand cycles can be performed without noticeable loss.

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