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2,4-Dichloro-3-methylbenzoic acid is an organic compound that belongs to the class of phenylpropanoids and polyketides. It is an aromatic compound characterized by the presence of a phenol or polyketide moiety substituted by one or more alkyl or aryl groups. The chemical structure features a benzene ring with two chlorine atoms (dichloro) at the 2nd and 4th positions and a methyl group attached to the 3rd position, along with a carboxylic acid functional group. 2,4-DICHLORO-3-METHYLBENZOIC ACID is known for its stability and rigidity due to its aromatic ring structure, and its reactivity and solubility are largely influenced by the functional groups present.

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  • 83277-23-0 Structure
  • Basic information

    1. Product Name: 2,4-DICHLORO-3-METHYLBENZOIC ACID
    2. Synonyms: 2,4-DICHLORO-3-METHYLBENZOIC ACID
    3. CAS NO:83277-23-0
    4. Molecular Formula: C8H6Cl2O2
    5. Molecular Weight: 205.03804
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83277-23-0.mol
    9. Article Data: 11
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 320.9±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.442±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 2.78±0.28(Predicted)
    10. CAS DataBase Reference: 2,4-DICHLORO-3-METHYLBENZOIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,4-DICHLORO-3-METHYLBENZOIC ACID(83277-23-0)
    12. EPA Substance Registry System: 2,4-DICHLORO-3-METHYLBENZOIC ACID(83277-23-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 83277-23-0(Hazardous Substances Data)

83277-23-0 Usage

Uses

Used in Chemical Synthesis:
2,4-Dichloro-3-methylbenzoic acid is used as a chemical intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable building block for creating new molecules with specific properties and applications.
Used in Industrial Manufacturing:
2,4-DICHLORO-3-METHYLBENZOIC ACID can be utilized in the production of various industrial products, such as dyes, plastics, and coatings. Its chemical properties, including reactivity and solubility, contribute to the performance and characteristics of the final products.
Used in Pharmaceuticals:
2,4-Dichloro-3-methylbenzoic acid has potential applications in the pharmaceutical industry, where it can be used as an active pharmaceutical ingredient or as a precursor in the synthesis of drug molecules. Its unique structure and functional groups may contribute to the development of new therapeutic agents.
Used as a Laboratory Reagent:
In research laboratories, 2,4-dichloro-3-methylbenzoic acid can serve as a reagent for various chemical reactions and experiments. Its properties and reactivity make it suitable for studying chemical processes and developing new synthetic methods.
It is important to handle 2,4-dichloro-3-methylbenzoic acid with care, considering its potential toxicity and corrosive properties. Proper safety measures should be taken during its use to minimize risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 83277-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,7 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83277-23:
(7*8)+(6*3)+(5*2)+(4*7)+(3*7)+(2*2)+(1*3)=140
140 % 10 = 0
So 83277-23-0 is a valid CAS Registry Number.

83277-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichloro-3-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2,4-Dichloro-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:83277-23-0 SDS

83277-23-0Relevant articles and documents

Substituted benzoyl compound and application thereof

-

, (2021/03/03)

The invention provides a substituted benzoyl compound and application thereof. Specifically, the invention provides a compound shown as a formula (I), a preparation method and application of the compound as a herbicide. Specifically, Q is optionally subst

Substituted benzoyl-pyrazole compounds and application thereof in agriculture

-

Paragraph 0180; 0185-0187, (2021/01/15)

The invention provides substituted benzoyl-pyrazole compounds and an application thereof in agriculture. Specifically, the invention provides the compounds represented by a formula (I) and a preparation method thereof. the invention discloses aompositions

5,6,7,8-TETRAHYDRO[1,2,4]TRIAZOLO[4,3-a]PYRAZINE DERIVATIVES AS P2X7 MODULATORS

-

Page/Page column 100, (2010/11/17)

The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof wherein A is hydrogen, C1-4alkyl, C3-6cycloalkyl, C1-3alkoxy, C1-3alkoxy C1-4alkyl, C1-2fluoroalkyl, halogen, NR6 R7, optionally substituted heteroaryl (Het), or optionally substituted phenyl, and R1, R2, R3, R4, R5, R6 and R7 are as defined in the description. The compounds or salts are thought to modulate P2X7 receptor function and to be capable of antagonizing the effects of ATP at the P2X7 receptor. The invention also provides the use of the compound or salt in the treatment or prophylaxis of, for example, inflammatory pain, neuropathic pain, visceral pain, rheumatoid arthritis, osteoarthritis or neurodegenerative disorders.

Proton mobility in 2-substituted 1,3-dichlorobenzenes: "ortho" or "meta" metalation?

Schlosser, Manfred,Heiss, Christophe,Marzi, Elena,Scopelliti, Rosario

, p. 4398 - 4404 (2007/10/03)

Nine 1,3-dichlorobenzene congeners were selected as model compounds to assess the relative rates of proton abstraction from 4- and 5-positions ("ortho" vs. "meta" metalation). Using lithium 2,2,6,6-tetramethylpiperidide as the basic reagent, the chlorine-adjacent 4-position underwent metalation exclusively. In contrast, attack at the chlorine-remote 5-posi" tion became significant even in the case of moderately sized 2-substituents (such as dimethylamino or ethyl) when secbutyllithium was employed. The "ortho/para" (4-/5-) ratios ranged from 80:20 to 65:35. The more pronounced "meta-orienting" effect of silicon as opposed to carbon substituents can be attributed to dissimilarities in the n polarization of the aromatic ring. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

COMPOUNDS HAVING ACTIVITY AT 5HT2C RECEPTOR AND USES THEREOF

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Page 19; 20; 26, (2010/02/09)

Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed: wherein R1 is halogen, cyano, C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkyloxy, C1-6alkoxy, C1 6alkylthio, hydroxy, amino, mono or di C1 6alkylamino, an N-linked 4 to 7 memb

Substituted 2-benzoyl-cyclohexan-1,3-diones with herbicidal effect

-

, (2008/06/13)

The invention relates to 2-benzoylcyclohexane-1,3-diones of the formula I where R1, R2are each hydrogen, nitro, halogen, cyano, thiocyanato, alkyl, haloalkyl, alkoxyalkyl, alkenyl, alkynyl, —OR5, —OCOR6, —OSOsu

Substituted 2-(3-alkenyl-benzoyl)-cyclohexane-1,3-diones

-

, (2008/06/13)

The invention relates to 2-(3-alkenylbenzoyl)cyclohexane-1,3-diones of the formula I where the variables have the following meanings: R1, R2are hydrogen, nitro, halogen, cyano, thiocyanato, alkyl, haloalkyl, alkoxyalkyl, alkenyl, alk

Substituted 4-benzoylpyrazoles

-

, (2008/06/13)

PCT No. PCT/EP97/07210 Sec. 371 Date Jun. 23, 1999 Sec. 102(e) Date Jun. 23, 1999 PCT Filed Dec. 19, 1997 PCT Pub. No. WO98/29392 PCT Pub. Date Jul. 9, 1998The invention relates to 4-benzoylpyrazoles of the formula I and their agriculturally useful salts

Substituted 4-(3-alkenylbenzoyl)pyrazoles

-

, (2008/06/13)

PCT No. PCT/EP98/02433 Sec. 371 Date Nov. 2, 1999 Sec. 102(e) Date Nov. 2, 1999 PCT Filed May 5, 1998 PCT Pub. No. WO98/50366 PCT Pub. Date Nov. 12, 19984-(3-Alkenylbenzoyl)pyrazoles of the formula I and agriculturally useful salts thereof; processes for preparing the compounds of the formula I; compositions comprising them; and the use of these derivatives or of compositions comprising them for controlling undesirable plants.

4-benzoylisoxazole herbicides

-

, (2008/06/13)

The invention relates to 4-benzoylisoxazole derivatives of formula (I): STR1 wherein: R represents the hydrogen atom or a group --CO2 R4 ; R1 represents alkyl, haloalkyl or optionally substituted cycloalkyl; R2

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