5-Bromoisoquinoline

Names

[ CAS No. ]:
34784-04-8

[ Name ]:
5-Bromoisoquinoline

[Synonym ]:
5-Bromoisoquinoline
Isoquinoline, 5-bromo-
5-bromo-isoquinoline
5-Brom-isochinolin
MFCD01646405

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
312.3±15.0 °C at 760 mmHg

[ Melting Point ]:
83-87 °C(lit.)

[ Molecular Formula ]:
C₉H₆BrN

[ Molecular Weight ]:
208.055

[ Flash Point ]:
142.7±20.4 °C

[ Exact Mass ]:
206.968353

[ PSA ]:
12.89000

[ LogP ]:
2.73

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.674

[ Storage condition ]:
Refrigerator

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R21/22;R36/37/38

[ Safety Phrases ]:
S26-S36-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933499090

Precursor & DownStream

Precursor

Isoquinoline
Isoquinolin-5-amine
N-[(3-Bromophenyl)methylene]-2,2-dimethoxyethanamine
Aqueous ammonia
3-Bromobenzaldehyde
2,2-Diethoxyethanamine
Sulfuric acid
(3-bromo-benzylidenamino)-acetaldehyde diethylacetal

DownStream

5-piperazin-1-ylisoquinoline
5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline
8-Chloroisoquinoline
Isoquinoline-5-boronicacid
5-Bromo-8-isoquinolinamine
5-Bromo-1-chloroisoquinoline
8-Aminoisoquinoline
Isoquinoline-5-carbaldehyde
Isoquinoline
5-(2,5-dimethylphenoxy)isoquinoline

Customs

[ HS Code ]: 2933499090

[ Summary ]:
2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Palladium-catalyzed coupling of ammonia and lithium amide with aryl halides.

J. Am. Chem. Soc. 128 , 10028, (2006)

A mild, palladium-catalyzed coupling of aryl halides with ammonia or lithium amide to form primary arylamines as the major product is described. These reactions occurred with excellent selectivity for...

Aminomethylations via cross-coupling of potassium organotrifluoroborates with aryl bromides.

Org. Lett. 9 , 1597, (2007)

[reaction: see text] The Suzuki-Miyaura cross-coupling reaction of N,N-dialkylaminomethyltrifluoroborates with aryl halides allows the construction of an aminomethyl aryl linkage through a disconnecti...

5-Bromoisoquinoline 2-oxide
8-Amino-5-bromoisoquinoline
1-Amino-5-bromoisoquinoline
6-amino-5-bromoisoquinoline
1-Chloro-5-bromoisoquinoline
3-Methyl-5-bromoisoquinoline
(3-Chloro-5-(pyrrolidine-1-carbonyl)phenyl)boronic acid
tert-butyl N-[4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carbonyl]phenyl]carbamate
Ethyl 7-methyl-1,2,3,4-tetrahydroisoquinoline-4-carboxylate
1,1-Dimethylethyl 6-fluoro-2-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
Ethyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyrimidine-3-carboxylate
3-[[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methoxy]phenol
2-[[3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]amino]acetamide
5-Methyl-1-oxo-2,3-dihydro-1H-indene-4-carboxylic acid
(5-Bromo-2-iodo-3-methoxyphenyl)methanol
5-Bromo-1-(bromomethyl)-2-iodo-3-methoxybenzene

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