8-Hydroxyjulolidine-9-carboxaldehyde - ≥96%(GC) , CAS No.63149-33-7

CAS: 63149-33-7 Cat. No.: H156880 Molecular Weight: 217.27 EC Number: 263-966-4
AVAILABLE TO ORDER
GRADE & PURITY ≥96%(GC)
Synonyms
9-Formyl-8-hydroxyjulolidine | SY050467 | Z1427939288 | 8-Hydroxyjulolidine-9-carboxaldehyde | AKOS000589073 | 2,3,6,7-Tetrahydro-8-hydroxy-1H,5H-benzo(ij)quinolizine-9-carboxaldehyde | 2,3,6,7-Tetrahydro-8-hydroxy-1H,5H-benzo[ij]quinolizine-9-carboxaldeh
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
H156880-1g
5
$33.90
5g
H156880-5g
5
$135.90
25g
H156880-25g
4
$585.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥96%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
9-Formyl-8-hydroxyjulolidine | SY050467 | Z1427939288 | 8-Hydroxyjulolidine-9-carboxaldehyde | AKOS000589073 | 2, 3, 6, 7-Tetrahydro-8-hydroxy-1H, 5H-benzo(ij)quinolizine-9-carboxaldehyde | 2, 3, 6, 7-Tetrahydro-8-hydroxy-1H, 5H-benzo[ij]quinolizine-9-carboxaldeh
Specifications & Purity
≥96%(GC)
Storage
Argon charged, Room temperature
Shipped In
Normal
Purity
≥96%(GC)
Names and Identifiers
Pubchem Sid504756704
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756704
Canonical SmilesC1CC2=CC(=C(C3=C2N(C1)CCC3)O)C=O
IUPAC Name6-hydroxy-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8-triene-7-carbaldehyde
InChIKeyNRZXBDYODHLZBF-UHFFFAOYSA-N
INCHI1S/C13H15NO2/c15-8-10-7-9-3-1-5-14-6-2-4-11(12(9)14)13(10)16/h7-8,16H,1-6H2
Isomeric SMILES C1CC2=CC(=C(C3=C2N(C1)CCC3)O)C=O
WGK Germany 3
Molecular Weight 217.27
Reaxy-Rn 3612337
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3612337&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassQuinolines and derivatives
SubclassHydroquinolines
Intermediate Tree Nodes Not available
Direct ParentHydroquinolines
Alternative Parents Dialkylarylamines  Aryl-aldehydes  Aralkylamines  Benzenoids  Vinylogous acids  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Tetrahydroquinoline - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aryl-aldehyde - Aralkylamine - Benzenoid - Vinylogous acid - Tertiary amine - Azacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Aldehyde - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
DLD-1 (17511 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SiHa (2051 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-87 MG (3946 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HUVEC (11049 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
B16 (5829 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NIH3T3 (5395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

9 results found

Lot NumberCertificate TypeDateItem
K2021042Certificate of AnalysisSep 11, 2024 H156880
E2615188Certificate of AnalysisOct 09, 2022 H156880
G2321107Certificate of AnalysisOct 09, 2022 H156880
I2516051Certificate of AnalysisOct 09, 2022 H156880
J2229195Certificate of AnalysisOct 09, 2022 H156880
J2229404Certificate of AnalysisOct 09, 2022 H156880
J2229405Certificate of AnalysisOct 09, 2022 H156880
L2418405Certificate of AnalysisOct 09, 2022 H156880
L2524132Certificate of AnalysisOct 09, 2022 H156880
Chemical and Physical Properties
Sensitivityair sensitive
Melt Point(°C)70.0to74.0°C
Molecular Weight217.260 g/mol
XLogP32.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass217.11 Da
Monoisotopic Mass217.11 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count16
Formal Charge0
Complexity281.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Kangming Xiong, Fangjun Huo, Yongbin Zhang, Ying Wen, Jianbin Chao, Caixia Yin.  (2017)  A novel recognition mechanism based on aldehyde group oxidized into carboxyl group by hypochlorite for the materials of fluorescent probes.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2017.09.042]
Solution Calculators
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