Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H7ClO |
Molecular Weight | 142.583 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(Cl)C(O)=C1
InChI
InChIKey=SMFHPCZZAAMJJO-UHFFFAOYSA-N
InChI=1S/C7H7ClO/c1-5-2-3-6(8)7(9)4-5/h2-4,9H,1H3
Molecular Formula | C7H7ClO |
Molecular Weight | 142.583 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/18986764Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/19800733 | https://www.ncbi.nlm.nih.gov/pubmed/19447466
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18986764
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/19800733 | https://www.ncbi.nlm.nih.gov/pubmed/19447466
2-Chloro-5-methylphenol is organic compound used in the synthesis of troarylpyrazoles as anti-cancer agents. 2-Chloro-5-Methylphenol is extensively used in the manufacture of resins, herbicides, pharmaceuticals, tricresylic acid surfactants. Wastewater from these industries together with coal-conversion unit and petrochemicals contain high concentration of cresol. Discharge of cresols into the environment poses significant health threat due to carcinogenic and refractory nature.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Supramolecular structures of 2-chloro-5-methylphenol and 4-chloro-3-methylphenol (chlorocresol). | 2003 Sep |
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Oxidation of p-chlorotoluene and cyclohexene catalysed by polymer-anchored oxovanadium(IV) and copper(II) complexes of amino acid derived tridentate ligands. | 2008 Aug 28 |
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N-Benzyl-2-(2-chloro-5-methyl-phen-oxy)acetamide. | 2008 Nov 22 |
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Synthesis of 2-(4-chlorophenyl)-2-(4-chloro-3-thiophenol)-1,1-dichloroethene (3-SH-DDE) via Newman-Kwart rearrangement - a precursor for synthesis of radiolabeled and unlabeled alkylsulfonyl-DDEs. | 2009 Aug |
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Thermophilic degradation of phenolic compounds in lab scale hybrid up flow anaerobic sludge blanket reactors. | 2009 May 30 |
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Sonochemical degradation of 2chloro-5methyl phenol assisted by TiO2 and H2O2. | 2010 Feb 15 |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.sciencelab.com/msds.php?msdsId=9923424
ORAL (LD50): Acute: 562 mg/kg [Birds.]
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:45:32 GMT 2023
by
admin
on
Sat Dec 16 08:45:32 GMT 2023
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Record UNII |
16Z94994Z4
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Record Status |
Validated (UNII)
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Record Version |
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