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4-Hydroxyindole - 98%, high purity , CAS No.2380-94-1

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4-Hydroxyindole - 98%, high purity , CAS No.2380-94-1

1 Citations

COA

Grade & Purity:

≥98%

Cas Number: 2380-94-1
Molecular Weight: 133.15
Beilstein Registry Number: 114905
EC Number: 219-177-2
MDL number: MFCD00005667
PubChem CID: 75421
PubChem SID: 488185099

In stock

Item Number

H105121

Grouped product items
SKU	Size	Availability	Price
H105121-1g	1g	5	$15.90
H105121-5g	5g	4	$55.90
H105121-25g	25g	4	$203.90
H105121-100g	100g	2	$731.90

View related series

azole (525) Biochemical Assay Reagents (928) Five-Membered Heterocyclic Compounds (2064)

Basic Description

Synonyms	STK802156 \| PS-3280 \| Z1203730747 \| 4-Indolol \| NCGC00253639-01 \| UNII-1W4VD9085V \| EINECS 219-177-2 \| 4-HYDROXYINDOLE [USP-RS] \| 82CYO8A460 \| Indol-4-ol \| SR-01000944737-1 \| AC-5462 \| AM20060360 \| SY001960 \| 4-Hydroxyindole, 99% \| CCG-214548 \| SR-0100094
Specifications & Purity	≥98%
Storage Temp	Argon charged
Shipped In	Normal
Product Description	· Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes · Reactant for preparation of small molecules targeting interaction between HIV-1 integrase and LEDGF/p75 cofactor · Reactant for preparation of dopamine D2 receptor antagonists · Reactant for preparation of SCD inhibitor MF-438 · Reactant for preparation of carbon-11-labeled 4-aryl-4H-chromenes as new PET agents for imaging of apoptosis in cancer · Reactant for preparation of indole/quinoline carbothioic acid amide derivatives as HCV inhibitors

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Indoles and derivatives
    - Subclass Hydroxyindoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Indoles and derivatives
Subclass	Hydroxyindoles
Intermediate Tree Nodes	Not available
Direct Parent	Hydroxyindoles
Alternative Parents	Indoles 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Hydroxyindole - Indole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group.
External Descriptors	phenols - hydroxyindoles
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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	488185099
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488185099
IUPAC Name	1H-indol-4-ol
INCHI	InChI=1S/C8H7NO/c10-8-3-1-2-7-6(8)4-5-9-7/h1-5,9-10H
InChIKey	NLMQHXUGJIAKTH-UHFFFAOYSA-N
Smiles	C1=CC2=C(C=CN2)C(=C1)O
Isomeric SMILES	C1=CC2=C(C=CN2)C(=C1)O
WGK Germany	3
Molecular Weight	133.15
Beilstein	114905
Reaxy-Rn	114905
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114905&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.

8 results found

Lot Number	Certificate Type	Date	Item
G2027101	Certificate of Analysis	May 08, 2024	H105121
D2428278	Certificate of Analysis	Mar 23, 2024	H105121
C1918158	Certificate of Analysis	Jan 15, 2023	H105121
J2226708	Certificate of Analysis	Sep 01, 2022	H105121
J2226618	Certificate of Analysis	Sep 01, 2022	H105121
J2226456	Certificate of Analysis	Sep 01, 2022	H105121
J2226455	Certificate of Analysis	Sep 01, 2022	H105121
E1816108	Certificate of Analysis	Apr 01, 2022	H105121

Chemical and Physical Properties

Sensitivity	air sensitive
Melt Point(°C)	99°C
Molecular Weight	133.150 g/mol
XLogP3	2.400
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	133.053 Da
Monoisotopic Mass	133.053 Da
Topological Polar Surface Area	36.000 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	126.000
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

How to Cite Aladdin Scientific Products?

1. Longfei Zhang, Li Yang, Yewei Xu, Guanjun Chang. (2019) Renewable 4-HIF/NaOH aerogel for efficient methylene blue removal via cation–π interaction induced electrostatic interaction. RSC Advances, 9 (51): (29772-29778).

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