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8-HYDROXYJULOLIDINE

CAS No.
41175-50-2
Chemical Name:
8-HYDROXYJULOLIDINE
Synonyms
2,3,6,7-TETRAHYDRO-1H,5H-PYRIDO[3,2,1-IJ]QUINOLIN-8-OL;AKOS BBS-00000819;8-HYDROXYJULOLIDINE;TIMTEC-BB SBB006615;8-HydroxyIulolidineHCl;8-Hydroxyjulolidine>8-Hydroxyjulolidine,98%;8-HYDROXYJULOLIDINE HYDROCHLORIDE;2,3,6,7-TETRAHYDRO-1H,5H-BENZO[I,J]-QUIN;1,2,3,5,6,7-Hexahydropyrido[3,2,1-ij]quin
CBNumber:
CB8445281
Molecular Formula:
C12H15NO
Molecular Weight:
189.25
MDL Number:
MFCD00006918
MOL File:
41175-50-2.mol
Last updated:2025-07-24 18:13:47
Product description Number Pack Size Price
8-Hydroxyjulolidine 97% 249394 1g $107
8-Hydroxyjulolidine 97% 249394 5g $348.65
8-Hydroxyjulolidine >97.0%(HPLC)(T) H0928 1g $55
8-Hydroxyjulolidine >97.0%(HPLC)(T) H0928 5g $187
8-Hydroxyjulolidine H943675 250mg $145
More product size

8-HYDROXYJULOLIDINE Properties

Melting point 132-134 °C(lit.)
Boiling point 374.4±41.0 °C(Predicted)
Density 1.22±0.1 g/cm3(Predicted)
storage temp. room temp
solubility Chloroform (Slightly), Methanol (Slightly)
pka 11.25±0.20(Predicted)
form Solid
color White to Pink
Water Solubility Soluble in water (partly), ethanol, chloroform, methanol, and acetone.
BRN 1530423
InChI InChI=1S/C12H15NO/c14-11-6-5-9-3-1-7-13-8-2-4-10(11)12(9)13/h5-6,14H,1-4,7-8H2
InChIKey FOFUWJNBAQJABO-UHFFFAOYSA-N
SMILES C12=CC=C(O)C3=C1N(CCC3)CCC2
CAS DataBase Reference 41175-50-2(CAS DataBase Reference)
FDA UNII SDF5635X33
EPA Substance Registry System 1H,5H-Benzo[ij]quinolizin-8-ol, 2,3,6,7-tetrahydro- (41175-50-2)
UNSPSC Code 12352104
NACRES NA.47

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-37/39-26-36
WGK Germany  3
10
TSCA  Yes
HS Code  2933 99 80
NFPA 704
1
2 0

8-HYDROXYJULOLIDINE price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 249394 8-Hydroxyjulolidine 97% 41175-50-2 1g $107 2025-07-31 Buy
Sigma-Aldrich 249394 8-Hydroxyjulolidine 97% 41175-50-2 5g $348.65 2025-07-31 Buy
TCI Chemical H0928 8-Hydroxyjulolidine >97.0%(HPLC)(T) 41175-50-2 1g $55 2025-07-31 Buy
TCI Chemical H0928 8-Hydroxyjulolidine >97.0%(HPLC)(T) 41175-50-2 5g $187 2025-07-31 Buy
TRC H943675 8-Hydroxyjulolidine 41175-50-2 250mg $145 2021-12-16 Buy
Product number Packaging Price Buy
249394 1g $107 Buy
249394 5g $348.65 Buy
H0928 1g $55 Buy
H0928 5g $187 Buy
H943675 250mg $145 Buy

8-HYDROXYJULOLIDINE Chemical Properties,Uses,Production

Chemical Properties

pink to beige or brown fine crystalline powder

Uses

8-Hydroxyjulolidine is used as an intermediate in the preparation of aminocoumarins via microwave-accelerated Pechmann reaction. It is also employed as a starting material for coumarin C-ribosides.

Uses

8-Hydroxyjulolidine has been used in the electrochemical switching fluorescence study.

General Description

The carboxaldehyde derivative of 8-hydroxyjulolidine is useful as a chromophore in fluorescence chemosensor and chemosensors.

Synthesis

8-Methoxyjulolidine

63468-83-7

8-HYDROXYJULOLIDINE

41175-50-2

The general procedure for the synthesis of 1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-8-ol from 8-methoxyjulolidine was as follows: 8-methoxyjulolidine (10 g, 50 mmol) was dissolved in a mixed solution consisting of 50 mL of 47% hydriodic acid, 80 mL of concentrated hydrochloric acid and 200 mL of water. The reaction mixture was heated to reflux and the progress of the reaction was monitored by thin layer chromatography (TLC). After 15 hours of reaction, 50 mL of concentrated hydrochloric acid was added to the mixture. The total reaction time was 60 hours. Upon completion of the reaction, the solution was cooled in an ice bath and first neutralized to pH 6 with 50% sodium hydroxide solution, followed by the addition of phosphate buffer (prepared by dissolving 6.9 g NaH2PO4-H2O and 1.4 g Na2HPO4 in 100 mL of water). The product was extracted with dichloromethane and the organic phase was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The resulting crude product was redissolved in dichloromethane and extracted repeatedly with 10% sodium hydroxide solution until the aqueous phase was colorless. Subsequently, the organic phase was acidified, dried and extracted again, and the solvent was removed as described above, resulting in the product 1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-8-ol (6.24 g) in 67% yield and with a melting point of 126-130°C. The product was extracted with sodium sulfate under reduced pressure.

References

[1] Journal of Organic Chemistry, 1987, vol. 52, # 8, p. 1465 - 1468
[2] Journal of Fluorescence, 2015, vol. 25, # 6, p. 1615 - 1628
[3] Chemical Communications, 2011, vol. 47, # 47, p. 12691 - 12693
[4] Chemistry - A European Journal, 2014, vol. 20, # 12, p. 3510 - 3519
[5] Patent: US2018/280543, 2018, A1. Location in patent: Paragraph 0041; 0098

8-HYDROXYJULOLIDINE Preparation Products And Raw materials

Global( 246)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-29-81148696 +86-17392712697 1022@dideu.com China 3996 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 20183 58
Springchem New Material Technology Co.,Limited
+86-021-62885108 +8613917661608 info@spring-chem.com China 2068 57
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29852 58
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10406 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49975 58
Zhengzhou Alfa Chemical Co.,Ltd
+8618530059196 sale04@alfachem.cn China 12089 58
Shanghai Rlavie Technology Co ltd
+86-021-67759270 +8617717059219 sales@rlavie.com China 1030 58

View Lastest Price from 8-HYDROXYJULOLIDINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
8-Hydroxyjulolidine pictures 2025-09-25 8-Hydroxyjulolidine
41175-50-2
US $200.00-1.00 / KG 1KG 99%, 99.5% Sublimated g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
8-HYDROXYJULOLIDINE pictures 2025-07-25 8-HYDROXYJULOLIDINE
41175-50-2
US $0.00-0.00 / kg 1kg 98% kgs Shaanxi Dideu New Materials Co. Ltd
8-HYDROXYJULOLIDINE pictures 2024-08-05 8-HYDROXYJULOLIDINE
41175-50-2
US $0.10 / KG 1KG 98.0% 10 Shaanxi Dideu Medichem Co. Ltd
  • 8-Hydroxyjulolidine pictures
  • 8-Hydroxyjulolidine
    41175-50-2
  • US $200.00-1.00 / KG
  • 99%, 99.5% Sublimated
  • Henan Fengda Chemical Co., Ltd
2,3,6,7-Tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-ol 97% AKOS BBS-00000819 8-HYDROXY-2,3,6,7-TETRAHYDRO-1H,5H-BENZO[IJ]QUINOLIZINE 8-HYDROXYJULOLIDINE 8-HYDROXYJULOLIDINE HYDROCHLORIDE 2,3,6,7-TETRAHYDRO-1H,5H-BENZO[IJ]QUINOLIZIN-8-OL 2,3,6,7-TETRAHYDRO-1H,5H-PYRIDO[3,2,1-IJ]QUINOLIN-8-OL 8-HydroxyIulolidineHCl 1H,5H-Benzoijquinolizin-8-ol, 2,3,6,7-tetrahydro- 8-Hydroxyjulolidine,98% 2,3,6,7-TETRAHYDRO-1H,5H-BENZO[I,J]-QUIN 1,2,3,5,6,7-Hexahydropyrido[3,2,1-ij]quinolin-8-ol 2,3,6,7-Tetrahydro-1H,5H-benzo[i,j]-quinolizin-8-ol for synthesis 2,3,6,7-Tetrahydro-1H,5H-benzop[ij]quinolizine-8-ol TIMTEC-BB SBB006615 ,3,6,7-Tetrahydro-1H,5H-benzo(ij)quinolizin-8-ol ,3,6,7-Tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-ol 5h-benzo[ij]quinolizin-8-ol,2,3,6,7-tetrahydro-1 8-Hydroxyjulolidine> 1,2,3,5,6,7-Hexahydropyrido[3,2,1-ij]quin 1-azatricyclo[7.3.1.0?13]trideca-5(13),6,8-trien-6-ol 1-azatricyclo7.3.1.0^{5,13}trideca-5,7,9(13)-trien-6-ol 41175-50-2 ALCOHOL Building Blocks Organic Building Blocks Oxygen Compounds Phenols