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2-Bromo-5-methoxy-3-methylbenzoic acid is a chemical compound characterized by its molecular formula C9H9BrO3. It is a white to off-white crystalline solid known for its bromo and methoxy functional groups, which contribute to its reactivity and biological activity. 2-BROMO-5-METHOXY-3-METHYLBENZOIC ACID is a valuable building block in the field of medicinal chemistry and drug discovery, commonly used in the synthesis of pharmaceuticals and agrochemicals.

174417-54-0

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174417-54-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-5-methoxy-3-methylbenzoic acid is used as an intermediate in organic synthesis for the production of various drugs and other organic compounds. Its unique structure and properties make it a promising candidate in the development of new pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Bromo-5-methoxy-3-methylbenzoic acid is utilized as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and biological activity contribute to the effectiveness of these compounds in controlling pests and promoting crop growth.

Check Digit Verification of cas no

The CAS Registry Mumber 174417-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,1 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 174417-54:
(8*1)+(7*7)+(6*4)+(5*4)+(4*1)+(3*7)+(2*5)+(1*4)=140
140 % 10 = 0
So 174417-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO3/c1-5-3-6(13-2)4-7(8(5)10)9(11)12/h3-4H,1-2H3,(H,11,12)

174417-54-0SDS

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 2-BROMO-5-METHOXY-3-METHYLBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 2-bromo-5-methoxy-3-methyl-benzoic 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:174417-54-0 SDS

174417-54-0Relevant articles and documents

Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions

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, (2008/06/13)

Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.

New 2,2′-substituted 4,4′-dimethoxy-6,6′-dimethyl[1, 1′-biphenyls], inducing a strong helical twisting power in liquid crystals

Holzwarth, Richard,Bartsch, Richard,Cherkaoui, Zoubair,Solladie, Guy

, p. 3931 - 3935 (2007/10/03)

Based on the stabilisation of the molecular motion by the chiral residue, novel optically active biphenylic chiral dopants for nematic liquid crystals were developed. This molecular congestion was obtained by introducing mesogenic residues on the 2,2′-positions of the chiral biphenyl; this led to a novel molecular architecture that was found to be efficient. The synthesised optically active biphenyls were characterised with very short cholesteric pitches when used as chiral dopants in nematic liquid crystals. The synthesis of the enatiomerically pure biphenyl dopants and their preliminary physicochemical characterisations are described.

NOVEL THIOPHENE AMIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATING COMPLEMENT-MEDIATED DISEASES AND CONDITIONS

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Page 268, (2010/02/05)

Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula (I) or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.

A New Family of Enantiomerically Pure Smectic C* Liquid Crystals with a Bridged Chiral Biphenyl Core

Solladie, Guy,Hugele, Philippe,Bartsch, Richard

, p. 3895 - 3898 (2007/10/03)

The synthesis of enantiomerically pure bridged biphenyl compounds, (-)-(R)-3,9-bis(4-(dodecyloxy)benzoyloxy)-5,7-dihydro-1,11-dimethyldibenzo[c,e] thiepine, 13, and (-)-(R)-3,9-bis(4-(dodecyloxy)benzoyloxy)-5,7-dihydro-1,11-dimethyldibenzo[c,e]- thiepin d

SYNTHESIS OF OPTICALLY ACTIVE O,O,O-TRIMETHYLKORUPENSAMINES A AND B

Rao, A. V. Rama,Gurjar, Mukund K.,Ramana, D. Venkata,Chheda, Abhay K.

, p. 1 - 6 (2007/10/02)

Hydrolysis of benzofuran derivative (10) with concomitant aromatisation produced the biaryl system (11).Subsequent Sharpless asymmetric epoxidation of the cinnamyl alcohol (13) gave atropisomers (14) and (15) conveniently separated by chromatography.Indep

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