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7-Hydroxycoumarin-4-acetic Acid - ≥97%, high purity , CAS No.6950-82-9

    Grade & Purity:
  • ≥97%
In stock
Item Number
H133558
Grouped product items
SKU Size
Availability
Price Qty
H133558-1g
1g
10
$35.90
H133558-5g
5g
3
$108.90
H133558-10g
10g
3
$194.90
H133558-25g
25g
4
$438.90
H133558-100g
100g
1
$1,579.90

Basic Description

Synonyms 7-Hydroxycoumarinyl-4-acetic acid | EN300-186397 | NSC 65625 | DTXSID50943938 | VELNACRINE [MI] | NSC642907 | NSC-642907 | 2H-1-Benzopyran-4-acetic acid, 7-hydroxy-2-oxo- | 7-Hydroxycoumarinyl-4-acetic acid, 97% | EINECS 204-249-8 | Umbelliferone-4-acetic
Specifications & Purity ≥97%
Storage Temp Argon charged
Shipped In Normal
Product Description

Usually used in the synthesis of novel and specific enzyme substrates for Maroteaux-Lamy (MPS VI) and Morquio A (MPS IVA) diseases, and also employed as ionic liquid matrice for MALDI-TOF MS of proteins, peptides and carbohydrates.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Phenylpropanoids and polyketides
Class Coumarins and derivatives
Subclass Hydroxycoumarins
Intermediate Tree Nodes Not available
Direct Parent 7-hydroxycoumarins
Alternative Parents 1-benzopyrans  Pyranones and derivatives  1-hydroxy-2-unsubstituted benzenoids  Heteroaromatic compounds  Lactones  Oxacyclic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents 7-hydroxycoumarin - Benzopyran - 1-benzopyran - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Organic oxide - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as 7-hydroxycoumarins. These are coumarins that contain one or more hydroxyl groups attached to the C7 position the coumarin skeleton.
External Descriptors Not available

Associated Targets(Human)

AKR1B1 Tclin Aldose reductase (1404 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
LCK Tclin Tyrosine-protein kinase LCK (9212 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SORD Tchem Sorbitol dehydrogenase (133 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FYN Tclin Tyrosine-protein kinase FYN (5308 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HT-29 (80576 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HepG2 (196354 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Grb2 Growth factor receptor-bound protein 2 (49 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
B16-F10 (4610 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488195376
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195376
IUPAC Name 2-(7-hydroxy-2-oxochromen-4-yl)acetic acid
INCHI InChI=1S/C11H8O5/c12-7-1-2-8-6(3-10(13)14)4-11(15)16-9(8)5-7/h1-2,4-5,12H,3H2,(H,13,14)
InChIKey BNHPMQBVNXMPDU-UHFFFAOYSA-N
Smiles C1=CC2=C(C=C1O)OC(=O)C=C2CC(=O)O
Isomeric SMILES C1=CC2=C(C=C1O)OC(=O)C=C2CC(=O)O
WGK Germany 3
Molecular Weight 220.18
Beilstein 204777
Reaxy-Rn 204777
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=204777&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot Number Certificate Type Date Item
L2419136 Certificate of Analysis Dec 27, 2024 H133558
L2419135 Certificate of Analysis Dec 27, 2024 H133558
L2423076 Certificate of Analysis Jul 08, 2024 H133558
L2423210 Certificate of Analysis Jul 08, 2024 H133558
L2423211 Certificate of Analysis Jul 08, 2024 H133558
H2218334 Certificate of Analysis Jun 17, 2024 H133558
H2218336 Certificate of Analysis Jun 17, 2024 H133558
H2218335 Certificate of Analysis Jun 17, 2024 H133558
H2218337 Certificate of Analysis Jun 17, 2024 H133558
H2218338 Certificate of Analysis Jun 17, 2024 H133558
D1514011 Certificate of Analysis Nov 16, 2022 H133558
D1924040 Certificate of Analysis Nov 11, 2022 H133558
G2213574 Certificate of Analysis Jul 16, 2022 H133558
D23142390 Certificate of Analysis Jul 16, 2022 H133558
C2218010 Certificate of Analysis Mar 22, 2022 H133558

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Chemical and Physical Properties

Solubility Soluble in Methanol
Melt Point(°C) 190 °C(dec.)
Molecular Weight 220.180 g/mol
XLogP3 1.000
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 2
Exact Mass 220.037 Da
Monoisotopic Mass 220.037 Da
Topological Polar Surface Area 83.800 Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 346.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Na Wen, Chunmei Gao, Shaoyu Lü, Xiubin Xu, Xiao Bai, Can Wu, Piao Ning, Shaofei Zhang, Mingzhu Liu.  (2017)  Novel amphiphilic glucose-responsive modified starch micelles for insulin delivery.  RSC Advances,  (73): (45978-45986). 

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