ChemicalBook > CAS DataBase List > 6-BROMO-4-IODOQUINOLINE

6-BROMO-4-IODOQUINOLINE

Product Name
6-BROMO-4-IODOQUINOLINE
CAS No.
927801-23-8
Chemical Name
6-BROMO-4-IODOQUINOLINE
Synonyms
6-BROMO-4-IODOQUINOLINE;4-Iodo-6-bromoquinoline;Quinoline, 6-bromo-4-iodo-;6-Bromo-4-iodoquinoline 97%
CBNumber
CB1222641
Molecular Formula
C9H5BrIN
Formula Weight
333.95
MOL File
Mol file
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6-BROMO-4-IODOQUINOLINE Property

Boiling point:
375.5±22.0 °C(Predicted)
Density 
2.154±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
solid
pka
2.77±0.16(Predicted)
color 
Brown
InChI
InChI=1S/C9H5BrIN/c10-6-1-2-9-7(5-6)8(11)3-4-12-9/h1-5H
InChIKey
BWFLFNVNIISPPK-UHFFFAOYSA-N
SMILES
N1C2C(=CC(Br)=CC=2)C(I)=CC=1
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Safety

HS Code 
2933491090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P310Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

TRC
Product number
B693718
Product name
6-Bromo-4-iodoquinoline
Packaging
250mg
Price
$75
Updated
2021/12/16
Apolloscientific
Product number
OR927338
Product name
6-Bromo-4-iodoquinoline
Purity
97%
Packaging
1g
Price
$91
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB142388
Product name
6-Bromo-4-iodoquinoline
Packaging
500mg
Price
$110
Updated
2021/12/16
Apolloscientific
Product number
OR927338
Product name
6-Bromo-4-iodoquinoline
Purity
97%
Packaging
250mg
Price
$32
Updated
2021/12/16
SynQuest Laboratories
Product number
3H32-S-0B
Product name
6-Bromo-4-iodoquinoline
Purity
97%
Packaging
250mg
Price
$52
Updated
2021/12/16
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6-BROMO-4-IODOQUINOLINE Chemical Properties,Usage,Production

Synthesis

1086062-75-0

927801-23-8

4.1.9 Synthesis of 6-bromo-4-iodoquinoline (12): To an anhydrous ethyl acetate (20 mL) solution of 6-bromo-4-chloroquinoline (11) (3.50 g, 14.46 mmol) was added hydrochloric acid saturated ethyl acetate (40 mL), and the formation of a white precipitate was immediately observed. After stirring for 30 min, the suspension was concentrated under vacuum to give 6-bromo-4-chloroquinoline hydrochloride as an off-white solid (3.91 g, 14.14 mmol). Subsequently, 6-bromo-4-chloroquinoline hydrochloride (3.91 g, 14.14 mmol), anhydrous potassium iodide (9.76 g, 70.70 mmol), and anhydrous acetonitrile (100 mL) were added in a two-neck flask. The resulting slurry was stirred under reflux conditions for 48 hours and then cooled to room temperature. The reaction mixture was treated with saturated aqueous sodium bicarbonate solution (40 mL) and 5% sodium sulfite solution (20 mL). The reaction mixture was extracted with dichloromethane (200 mL x 2), and the combined organic phases were dried over magnesium sulfate and concentrated under vacuum to give the crude product. The crude product was further purified by silica gel column chromatography (25% ethyl acetate/petroleum ether) to afford the target compound 6-bromo-4-iodoquinoline (4.42 g, 13.27 mmol, 94% yield) as an off-white solid. 1H NMR (500 MHz, DMSO-d6) δ 8.51 (d, J = 4.5 Hz, 1H, Ar-H), 8.21 (d, J = 4.5 Hz, 1H, Ar-H), 8.11 (t, J = 1.5 Hz, 1H, Ar-H), 7.97-7.91 (m, 2H, Ar-H). ESI-MS: m/z = 334 [M + H]+.

References

[1] European Journal of Medicinal Chemistry, 2015, vol. 99, p. 36 - 50
[2] RSC Advances, 2017, vol. 7, # 4, p. 2342 - 2350
[3] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 4, p. 1569 - 1574
[4] Patent: WO2014/22128, 2014, A1. Location in patent: Paragraph 0156; 0157
[5] Patent: CN103539777, 2016, B. Location in patent: Paragraph 0276; 0327; 0328

6-BROMO-4-IODOQUINOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

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6-BROMO-4-IODOQUINOLINE Suppliers

Hefei Ruiluo New Material Technology Co., Ltd.
Tel
19567218739
Email
1759672789@qq.com
Country
China
ProdList
868
Advantage
58
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
18270980682
Fax
021 51613951
Email
mlcheng@sunwaypharm.cn
Country
China
ProdList
8669
Advantage
57
Chiba Pharmaceutical Science and technology Co, Ltd.
Tel
0531-81313138 13066006660
Fax
QQ: 3366077777
Email
chibapharm@foxmail.com
Country
China
ProdList
3991
Advantage
55
NovoChemy Ltd.
Tel
021-31261262/ 49 (0)17662837245
Fax
(0)21-33250524
Email
sales@novochemy.com
Country
Germany
ProdList
6328
Advantage
58
Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Fax
(86) 21-58955996
Email
info@chemexpress.com
Country
China
ProdList
7552
Advantage
61
Shanghai Raise Chemical Technology Co.,Ltd
Tel
15026594951
Fax
0556-5030632
Email
rs@raise-chem.com
Country
China
ProdList
4454
Advantage
55
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
ShangHai AmK Pharmaceutical Technology Co., Ltd.
Tel
微信 17321281695 18019252918
Fax
17321281695
Email
sale@amkchem.com
Country
China
ProdList
15136
Advantage
55
Shanghai XinKai Chemical Technology Co., Ltd.
Tel
021-58930698 15921516558
Fax
86-021-58933679
Email
zhangyichao84@126.com
Country
China
ProdList
981
Advantage
55
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View Lastest Price from 6-BROMO-4-IODOQUINOLINE manufacturers

Career Henan Chemical Co
Product
6-BROMO-4-IODOQUINOLINE 927801-23-8
Price
US $1.00/KG
Min. Order
1KG
Purity
95-99%
Supply Ability
1ton
Release date
2020-01-02

927801-23-8, 6-BROMO-4-IODOQUINOLINERelated Search:


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  • 4-Iodo-6-bromoquinoline
  • 927801-23-8
  • 27801-23-8