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2-BROMO-4-TERT-BUTYLBENZOIC ACID is a chemical compound characterized by its molecular formula C11H13BrO2. It is a white solid known for its strong acidic properties and is utilized in various applications across the pharmaceutical and chemical industries.

6332-96-3

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6332-96-3 Usage

Uses

Used in Organic Synthesis:
2-BROMO-4-TERT-BUTYLBENZOIC ACID is used as a building block for the synthesis of other organic compounds, particularly pharmaceutical intermediates, due to its versatile chemical structure and reactivity.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-BROMO-4-TERT-BUTYLBENZOIC ACID is used as a reagent in the preparation of various substituted benzoic acid derivatives, which are essential for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
2-BROMO-4-TERT-BUTYLBENZOIC ACID is also employed in the agrochemical sector for the synthesis of compounds with potential applications in crop protection and pest control.
Used in Polymer and Resin Production:
Due to its strong acidic properties, 2-BROMO-4-TERT-BUTYLBENZOIC ACID is utilized in the production of certain polymers and resins, contributing to the development of materials with specific properties for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6332-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6332-96:
(6*6)+(5*3)+(4*3)+(3*2)+(2*9)+(1*6)=93
93 % 10 = 3
So 6332-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H13BrO2/c1-11(2,3)7-4-5-8(10(13)14)9(12)6-7/h4-6H,1-3H3,(H,13,14)

6332-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-4-(tert-butyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-bromo-4-tert-butylbenzoic acid

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:6332-96-3 SDS

6332-96-3Relevant academic research and scientific papers

Cruciform Electron Acceptors Based on Tetraindeno-Fused Spirofluorene

Xia, Debin,Guo, Xin,Wagner, Manfred,Baumgarten, Martin,Schollmeyer, Dieter,Müllen, Klaus

, p. 2816 - 2821 (2017)

Two cruciform tetraindenospirofluorene-based acceptors embedding carbonyl (Spiro-4O) and dicyanovinylene (Spiro-8CN) functionalities are synthesized in high yields. Single-crystal X-ray analysis reveals a one-dimensional π-π stacking arrangement for Spiro

Organic compound with tetrahedral-like geometry

-

, (2018/03/25)

An organic compound with a tetrahedral-like geometry is disclosed. The organic compound has a structure represented by formula (I): wherein A1 to A4 each independently represent a 5-membered or 6-membered unsaturated ring; B1 represents direct bonding, —C—, —O—, —N—, —S— or —C═C—; m is 0 or 1; each of Ra's is independently hydrogen, fluorine, oxygen, substituted or unsubstituted C1-C12 alkyl or substituted or unsubstituted C6-C12 aryl; and n is an integer of 0 to 2.

Organic compound having tetrahedron-like configuration

-

, (2018/07/07)

The present invention relates to an organic compound having a tetrahedron-like configuration, wherein the organic compound has a structure represented by the following general formula (I) defined in the specification, A1-A4 are respectively and independently an unsaturated five-membered ring or an unsaturated six-membered ring, B is a direct bond , -C, -O-, -N-, -S-, or -C=C-, m is 0 or 1, Ris hydrogen, fluorine, substituted or unsubstituted C1-C12 alkyl, or substituted or unsubstituted C6-C12 aryl, and n is an integer of 0-2. The organic compound of the present invention has excellentphotoelectric property.

Synthesis of dilactone bridged terphenyls with crankshaft architectures

Dressler, Justin J.,Miller, Sarah A.,Meeuwsen, Brian T.,Riel, Asia Marie S.,Dahl, Bart J.

, p. 283 - 292 (2015/02/02)

Three highly fluorescent dilactone bridged terphenyls with crankshaft architectures have been synthesized. This general class of compounds is relatively unexplored. These compounds have been characterized by fluorescence and UV-vis spectroscopy. For all three compounds, a direct correlation between the rigidity of the terphenyl system and the strength of absorption and emission of light has been observed. Preliminary studies have indicated that compounds with this architecture have the potential to be useful as pH-driven molecular switches and/or sensors with instant fluorescence attenuation at high pH values.

Remote conformational control of a molecular switch via methylation and deprotonation

Knipe, Peter C.,Jones, Ian M.,Thompson, Sam,Hamilton, Andrew D.

supporting information, p. 9384 - 9388 (2014/12/11)

Exacting control over conformation in response to an external stimulus is the central focus of molecular switching. Here we describe the synthesis of a series of diphenylacetylene-based molecular switches, and examine their response to covalent modificati

Compositions useful as inhibitors of voltage-gated sodium channels

-

Page/Page column 45-46, (2008/06/13)

The present invention relates to compounds useful as inhibitors of voltage-gated sodium channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the t

Synthesis of a calix[5]arene receptor having two benzoic acid moieties

Haino, Takeharu,Nitta, Koji,Saijo, Yoshikazu,Matsumura, Kazumi,Hirakata, Masaki,Fukazawa, Yoshimasa

, p. 6301 - 6304 (2007/10/03)

Synthesis and binding behavior of a calix[5]arene receptor possessing two benzoic acids are reported. Two water molecules were bound within the cavity by hydrogen bonding interaction between the two carboxylic acids of the receptor. It also binds 2-aminopyrimidine to form a complex in which the aromatic ring of the guest resides deeply within the cavity.

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