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ChemicalBook >> CAS DataBase List >>5-Bromo-8-nitroisoquinoline

5-Bromo-8-nitroisoquinoline

CAS No.
63927-23-1
Chemical Name:
5-Bromo-8-nitroisoquinoline
Synonyms
5-BROMO-8-NITROISOQUINOLINE;5-BroMo-8-nitroisoquinolilne;Isoquinoline, 5-bromo-8-nitro-;5-Bromo-8-nitroisoquinoline >5-Bromo-8-nitroisoquinoline 90%;5-Bromo-8-nitroisoquinoline ISO 9001:2015 REACH
CBNumber:
CB1779655
Molecular Formula:
C9H5BrN2O2
Molecular Weight:
253.05
MDL Number:
MFCD02091227
MOL File:
63927-23-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:46:28
Product description Number Pack Size Price
5-Bromo-8-nitroisoquinoline 90% 675148 1g $51.9
5-Bromo-8-nitroisoquinoline >98.0%(GC)(T) B4163 1g $68
5-Bromo-8-nitroisoquinoline >97% OR41003 5g $21
5-Bromo-8-nitroisoquinoline >97% OR41003 25g $67
5-Bromo-8-nitroisoquinoline >97% OR41003 100g $243
More product size

5-Bromo-8-nitroisoquinoline Properties

Melting point 136-140 °C
Boiling point 386.9±27.0 °C(Predicted)
Density 1.747±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
pka 2+-.0.36(Predicted)
color Light yellow to Yellow to Orange
InChI 1S/C9H5BrN2O2/c10-8-1-2-9(12(13)14)7-5-11-4-3-6(7)8/h1-5H
InChIKey ULGOLOXWHJEZNZ-UHFFFAOYSA-N
SMILES [O-][N+](=O)c1ccc(Br)c2ccncc12
CAS DataBase Reference 63927-23-1(CAS DataBase Reference)
UNSPSC Code 12352100

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
Signal word  Danger
Hazard statements  H301-H315-H318
Precautionary statements  P280-P301+P310+P330-P302+P352-P305+P351+P338+P310
Hazard Codes  T
Risk Statements  25-37/38-41
Safety Statements  26-39-45
RIDADR  UN 2811
WGK Germany  3
HS Code  2933499090
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Eye Dam. 1
Skin Irrit. 2

5-Bromo-8-nitroisoquinoline price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 675148 5-Bromo-8-nitroisoquinoline 90% 63927-23-1 1g $51.9 2023-01-07 Buy
TCI Chemical B4163 5-Bromo-8-nitroisoquinoline >98.0%(GC)(T) 63927-23-1 1g $68 2026-04-30 Buy
Apolloscientific OR41003 5-Bromo-8-nitroisoquinoline >97% 63927-23-1 5g $21 2026-06-04 Buy
Apolloscientific OR41003 5-Bromo-8-nitroisoquinoline >97% 63927-23-1 25g $67 2026-06-04 Buy
Apolloscientific OR41003 5-Bromo-8-nitroisoquinoline >97% 63927-23-1 100g $243 2026-06-04 Buy
Product number Packaging Price Buy
675148 1g $51.9 Buy
B4163 1g $68 Buy
OR41003 5g $21 Buy
OR41003 25g $67 Buy
OR41003 100g $243 Buy

5-Bromo-8-nitroisoquinoline Chemical Properties,Uses,Production

Uses

5-Bromo-8-nitroisoquinoline is mainly used as an intermediate in organic synthesis and pharmaceutical chemistry, and can be used in the synthesis of drug molecules, pesticides, and dyes. In organic synthesis transformations, the bromine atom in 5-bromo-8-nitroisoquinoline can undergo debromination and hydrochemical oxidation under palladium and hydrogen conditions; in addition, the nitrogen atom on the isoquinoline ring can be oxidized to nitrogen oxides under the action of appropriate oxidizing agents.

Chemical Properties

It is light yellow solid powder under normal temperature and pressure, with certain alkalinity, can form salt with various acids.

Synthesis

5-Bromoisoquinoline

34784-04-8

5-Bromo-8-nitroisoquinoline

63927-23-1

Example 2: An aqueous solution of potassium nitrate (1.78 g, 8.56 mmol) was slowly added dropwise to a solution of 5-bromoisoquinoline dissolved in 12 mL of concentrated sulfuric acid. The reaction mixture was stirred at room temperature for 3 hours before it was poured into ice water and neutralized with concentrated ammonium hydroxide solution. The resulting yellow precipitate was extracted by ethyl acetate (3 x 10 mL) and the combined organic layers were washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtration, the organic phase was concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford 5-bromo-8-nitroisoquinoline in 96% yield using a hexane solution of 40% ethyl acetate as eluent.

References

[1] Patent: WO2004/76424, 2004, A1. Location in patent: Page 174-175
[2] Patent: EP698025, 1997, B1
[3] Patent: US5917053, 1999, A
[4] Patent: US5436250, 1995, A
[5] Patent: EP633262, 1995, A1

5-Bromo-8-nitroisoquinoline Preparation Products And Raw materials

Global( 234)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29640 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29812 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
Wuhan Chemwish Technology Co., Ltd
027-67849912 sales@chemwish.com CHINA 10821 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
+8613580539051 joe@yuhengpharm.com CHINA 21142 58
SIMAGCHEM CORP
+86-5922680277 +86-13806087780 sale@simagchem.com China 17346 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1059@dideu.com China 29094 58
Aston Chemical
-- sales@astonchem.com United States 1634 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52704 58

View Lastest Price from 5-Bromo-8-nitroisoquinoline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
5-Bromo-8-nitroisoquinoline  pictures 2025-11-18 5-Bromo-8-nitroisoquinoline
63927-23-1
$1.10 1g 99.00% 100 Tons Dideu Industries Group Limited
5-Bromo-8-nitroisoquinoline pictures 2019-07-06 5-Bromo-8-nitroisoquinoline
63927-23-1
$8.00 1KG 99% 10tons Career Henan Chemical Co

5-Bromo-8-nitroisoquinoline Spectrum

5-BROMO-8-NITROISOQUINOLINE Isoquinoline, 5-bromo-8-nitro- 5-BroMo-8-nitroisoquinolilne 5-Bromo-8-nitroisoquinoline 90% 5-Bromo-8-nitroisoquinoline > 5-Bromo-8-nitroisoquinoline ISO 9001:2015 REACH 63927-23-1 Halides Heterocycles Halogenated Heterocycles Heterocyclic Building Blocks Isoquinolines IsoquinolinesBuilding Blocks
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