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6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one

Base Information Edit
  • Chemical Name:6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one
  • CAS No.:19492-02-5
  • Molecular Formula:C10H7 Cl O3
  • Molecular Weight:210.61
  • Hs Code.:2932209090
  • European Community (EC) Number:832-456-9
  • DSSTox Substance ID:DTXSID20418744
  • Nikkaji Number:J2.394.155D
  • Wikidata:Q27467669
  • Metabolomics Workbench ID:74107
  • ChEMBL ID:CHEMBL2205240
  • Mol file:19492-02-5.mol
6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one

Synonyms:6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one;19492-02-5;6-chloro-7-hydroxy-4-methylcoumarin;6-chloro-7-hydroxy-4-methylchromen-2-one;CHEMBL2205240;6-chlor-4-methyl-7-hydroxy-cumarin;MFCD00816527;2H-1-Benzopyran-2-one,6-chloro-7-hydroxy-4-methyl-;XZZ;Oprea1_247174;Oprea1_602281;SCHEMBL2552748;DTXSID20418744;JTXAGHXRIBLWES-UHFFFAOYSA-N;4-Methyl-6-chloro-7-hydroxycoumarin;BBL029037;BDBM50555098;s5760;STK991554;AKOS000522583;AS-68431;PD098319;HY-128416;C3319;CS-0099278;FT-0705119;EN300-10318;T70505;2H-Chromen-2-one, 6-chloro-7-hydroxy-4-methyl-;6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one #;AN-829/25042006;Q27467669;Z57000606;6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one, AldrichCPR

Suppliers and Price of 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 6-Chloro-4-methylumbelliferone
  • 5g
  • $ 1075.00
  • TCI Chemical
  • 6-Chloro-7-hydroxy-4-methylcoumarin >98.0%(GC)
  • 5g
  • $ 464.00
  • TCI Chemical
  • 6-Chloro-7-hydroxy-4-methylcoumarin >98.0%(GC)
  • 1g
  • $ 134.00
  • Matrix Scientific
  • 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one
  • 500mg
  • $ 237.00
  • Crysdot
  • 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one 97%
  • 5g
  • $ 752.00
  • Chem-Impex
  • 6-Chloro-7-hydroxy-4-methylcoumarin,≥98%(GC) ≥98%(GC)
  • 1G
  • $ 160.28
  • Chemenu
  • 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one 97%
  • 5g
  • $ 711.00
  • Biosynth Carbosynth
  • 6-Chloro-7-hydroxy-4-methylcoumarin
  • 2 g
  • $ 250.00
  • Biosynth Carbosynth
  • 6-Chloro-7-hydroxy-4-methylcoumarin
  • 1 g
  • $ 150.00
  • Biosynth Carbosynth
  • 6-Chloro-7-hydroxy-4-methylcoumarin
  • 500 mg
  • $ 87.50
Total 7 raw suppliers
Chemical Property of 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one Edit
Chemical Property:
  • Vapor Pressure:1.35E-06mmHg at 25°C 
  • Melting Point:278 °C 
  • Boiling Point:388.7°Cat760mmHg 
  • Flash Point:188.9°C 
  • PSA:50.44000 
  • Density:1.447g/cm3 
  • LogP:2.46040 
  • Solubility.:soluble in Dimethylformamide 
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:210.0083718
  • Heavy Atom Count:14
  • Complexity:287
Purity/Quality:

98%,99%, *data from raw suppliers

6-Chloro-4-methylumbelliferone *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn 
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=O)OC2=CC(=C(C=C12)Cl)O
  • Uses 6-Chloro-4-methylumbelliferone is a fluorescent compound and its excitation and emission can be measured at 361 and 445 nm, respectively. It is used to develop novel fluorogenic substrates for the β-glycosidase assay.
Technology Process of 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one

There total 5 articles about 6-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With trifluoroacetic acid; at 100 ℃; for 0.5h; regioselective reaction; Microwave irradiation;
DOI:10.1002/chem.201201039
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