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ChemicalBook >> CAS DataBase List >>8-Bromoisoquinoline

8-Bromoisoquinoline

CAS No.
63927-22-0
Chemical Name:
8-Bromoisoquinoline
Synonyms
8-BromoisoquinoL;8-BROMOISOQUINOLINE;Isoquinoline, 8-bromo-;8-Bromoisoquinoline 95%;8-Bromoisoquinoline >8-Bromoisoquinoline ,97%;8-Bromo-isoquinoline()/98%/50g;8-Bromoisoquinoline ISO 9001:2015 REACH
CBNumber:
CB5217212
Molecular Formula:
C9H6BrN
Molecular Weight:
208.05
MDL Number:
MFCD04973298
MOL File:
63927-22-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 01:58:13
Product description Number Pack Size Price
8-Bromoisoquinoline >97.0%(GC)(T) B4144 1g $30
8-Bromoisoquinoline >97.0%(GC)(T) B4144 5g $117
8-Bromoisoquinoline ≥95% 10007082 500mg $37
8-Bromoisoquinoline ≥95% 10007082 1g $59
8-Bromoisoquinoline ≥99% 10007082 500mg $33
More product size

8-Bromoisoquinoline Properties

Melting point 80,5 C
Boiling point 312.3±15.0 °C(Predicted)
Density 1.564±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; Ethanol:PBS (pH 7.2) (1:8): .5 mg/ml
form powder to crystal
pka 4.63±0.23(Predicted)
color Light orange to Yellow to Green
InChI InChI=1S/C9H6BrN/c10-9-3-1-2-7-4-5-11-6-8(7)9/h1-6H
InChIKey DPRIHFQFWWCIGY-UHFFFAOYSA-N
SMILES C1C2=C(C=CC=C2Br)C=CN=1
CAS DataBase Reference 63927-22-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi,Xn,T
Risk Statements  36/37/38-20/21/22-25
Safety Statements  26-36-45
RIDADR  2811
Hazard Note  Irritant
HazardClass  6.1
PackingGroup 
HS Code  29334900
NFPA 704
0
2 0

8-Bromoisoquinoline price More Price(109)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical B4144 8-Bromoisoquinoline >97.0%(GC)(T) 63927-22-0 1g $30 2026-04-30 Buy
TCI Chemical B4144 8-Bromoisoquinoline >97.0%(GC)(T) 63927-22-0 5g $117 2026-04-30 Buy
Cayman Chemical 10007082 8-Bromoisoquinoline ≥95% 63927-22-0 500mg $37 2026-04-30 Buy
Cayman Chemical 10007082 8-Bromoisoquinoline ≥95% 63927-22-0 1g $59 2026-04-30 Buy
Cayman Chemical 10007082 8-Bromoisoquinoline ≥99% 63927-22-0 500mg $33 2024-03-01 Buy
Product number Packaging Price Buy
B4144 1g $30 Buy
B4144 5g $117 Buy
10007082 500mg $37 Buy
10007082 1g $59 Buy
10007082 500mg $33 Buy

8-Bromoisoquinoline Chemical Properties,Uses,Production

Chemical Properties

Yellow powder

Uses

8-Bromoisoquinoline is an intermediate used to prepare 4-((2-Hydroxy-3-methoxybenzyl)amino)benzenesulfonamide derivatives as potent and selective inhibitors of 12-Lipoxygenase. It is also used in the synthesis of selective excitatory amino acid transporter subtype 1 (EAAT1) Inhibitor UCPH-102.

Synthesis

2-Bromobenzaldehyde

6630-33-7

Aminoacetaldehyde dimethyl acetal

22483-09-6

8-Bromoisoquinoline

63927-22-0

1. 2-Bromobenzaldehyde (50 g, 270 mmol), aminoglyoxal dimethyl acetal (28.4 g, 270 mmol) and toluene (400 mL) were mixed under argon protection and heated to reflux. The dehydration reaction was carried out for 2.0 hours using a Dean-Stark apparatus. After dehydration was completed, reflux was continued for 1.0 hour. 2. Upon completion of the reaction, toluene was removed by evaporation under reduced pressure, the residue was dissolved in dichloromethane (600 mL), and the solution was cooled to 0°C. The reaction was then purged by evaporation under reduced pressure. 3. Aluminum chloride (118.9 g, 891.7 mmol) was slowly added to the cooled solution under argon protection, and the reaction mixture was then stirred at 45°C for 2.0 hours. 4. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the mixture was cooled to room temperature and slowly poured into ice water. 5. The dichloromethane layer was separated by alkalizing the mixture with 10% sodium hydroxide solution. The aqueous layer was re-extracted with dichloromethane (2 x 100mL). 6. The methylene chloride layer was combined, washed with brine and dried over anhydrous sodium sulfate. 7. The dichloromethane was removed by evaporation and the residue was purified by column chromatography on silica gel (100-200 mesh) to afford 8-bromoisoquinoline as an off-white solid (28 g, 49.8% yield) using a 5-8% ethyl acetate solution in hexane as the mobile phase. MS (ESI) m/z: 208 [M(79Br)+1], 210 [M(81Br)+1]; 1H NMR (400 MHz, DMSO-d6): δ 7.17 (t, J=7.8 Hz, 1H); 7.91 (d, J=6.0 Hz, 1H); 8.02 (d, J=8.4 Hz, 1H); 8.05 (d, J= 8.8 Hz, 1H); 8.65 (d, J=5.2 Hz, 1H); 9.48 (s, 1H).

References

[1] Patent: WO2016/21742, 2016, A1. Location in patent: Paragraph 0222; 0223

Global( 299)Suppliers
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Hebei Chuanghai Biotechnology Co., Ltd
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CONIER CHEM AND PHARMA LIMITED
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career henan chemical co
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View Lastest Price from 8-Bromoisoquinoline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
8-Bromoisoquinoline pictures 2026-07-02 8-Bromoisoquinoline
63927-22-0
$2.20-8.80 1kg 99%min 100kg ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
8-Bromoisoquinoline pictures 2026-03-20 8-Bromoisoquinoline
63927-22-0
$9.80 1KG 99% 10 tons Hebei Chuanghai Biotechnology Co., Ltd
8-Bromoisoquinoline  pictures 2025-11-18 8-Bromoisoquinoline
63927-22-0
$1.10 1g 99.00% 100 Tons Dideu Industries Group Limited

8-Bromoisoquinoline Spectrum

8-BROMOISOQUINOLINE 8-Bromoisoquinoline 95% Isoquinoline, 8-bromo- 8-Bromoisoquinoline ,97% 8-Bromoisoquinoline > 8-BromoisoquinoL 8-Bromoisoquinoline ISO 9001:2015 REACH 8-Bromo-isoquinoline()/98%/50g 63927-22-0 16567-18-2 Building Blocks Isoquinoline Quinolines, Isoquinolines & Quinoxalines Halides Quinolines, Isoquinolines & Quinoxalines Quinoline&Isoquinoline Isoquinoline Derivertives C8 to C10 Chemical Synthesis Heterocyclic Building Blocks New Products for Chemical Synthesis Heterocyclic Series blocks Bromides Heterocycles Quinolines Quinoline series
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