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ChemicalBook >> CAS DataBase List >>8-BROMO-2-CHLOROQUINAZOLINE

8-BROMO-2-CHLOROQUINAZOLINE

CAS No.
956100-63-3
Chemical Name:
8-BROMO-2-CHLOROQUINAZOLINE
Synonyms
2-chloro-8-bromoquinazoline;8-BROMO-2-CHLOROQUINAZOLINE;8-BroMo-2-chloroquinazoli...;Quinazoline, 8-bromo-2-chloro-;8-Bromo-2-chloroquinazoline 97%
CBNumber:
CB01517840
Molecular Formula:
C8H4BrClN2
Molecular Weight:
243.49
MDL Number:
MFCD11043845
MOL File:
956100-63-3.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:48

8-BROMO-2-CHLOROQUINAZOLINE Properties

Boiling point 309.7±24.0 °C(Predicted)
Density 1.762
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka -1.09±0.30(Predicted)
Appearance Yellow to orange Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
Risk Statements  41
Safety Statements  26-39
RIDADR  UN2811
HazardClass  IRRITANT
HS Code  2933998090

8-BROMO-2-CHLOROQUINAZOLINE price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B684733 8-Bromo-2-chloroquinazoline 956100-63-3 250mg $55 2021-12-16 Buy
Biosynth Carbosynth FB42522 8-Bromo-2-chloroquinazoline 956100-63-3 1g $425 2021-12-16 Buy
Medical Isotopes, Inc. 38143 8-Bromo-2-chloroquinazoline 95+% 956100-63-3 1g $495 2021-12-16 Buy
SynQuest Laboratories 3H32-D-88 8-Bromo-2-chloroquinazoline 956100-63-3 1g $608 2021-12-16 Buy
Biosynth Carbosynth FB42522 8-Bromo-2-chloroquinazoline 956100-63-3 2g $680 2021-12-16 Buy
Product number Packaging Price Buy
B684733 250mg $55 Buy
FB42522 1g $425 Buy
38143 1g $495 Buy
3H32-D-88 1g $608 Buy
FB42522 2g $680 Buy

8-BROMO-2-CHLOROQUINAZOLINE Chemical Properties,Uses,Production

Synthesis

4-Amino-8-bromo-2-chloroquinazoline

956100-62-2

8-BROMO-2-CHLOROQUINAZOLINE

956100-63-3

General procedure for the synthesis of 8-bromo-2-chloroquinazoline from 4-amino-8-bromo-2-chloroquinazoline: 8-bromo-2-chloroquinazolin-4-amine (12.93 g, 50 mmol) was dissolved in THF (500 mL) under stirring conditions, and isoamyl nitrite (23.43 g, 200 mmol) was added slowly dropwise over a dropwise period of 3 hours. Subsequently, the reaction mixture was continued to be stirred at 60 °C for 40 min. Upon completion of the reaction, the progress of the reaction was monitored by TLC (unfolding agent: PE:EA = 1:1). When the reaction was complete, the mixture was cooled to room temperature and the solvent was removed by distillation under reduced pressure. The residue was dissolved in DCM (300 mL) and the organic layer was washed sequentially with brine (100 mL) and water (100 mL). The organic layer was dried over anhydrous Na2SO4 and purified by column chromatography (eluent: DCM:PE = 1:1) to afford the target compound 8-bromo-2-chloroquinazoline as a yellow solid (8.21 g, 67% yield).1H NMR (DMSO-d6, 400 MHz): δ 9.66 (s, 1H), 8.45 (dd, J = 0.8, 7.6 Hz, 1H), 8.26 (dd, J = 0.8, 8.0 Hz, 1H), 7.73 (dd, J = 7.6, 8.0 Hz, 1H).

References

[1] Patent: WO2007/125405, 2007, A2. Location in patent: Page/Page column 25; 81-82
[2] Patent: EP3287463, 2018, A1. Location in patent: Paragraph 0191; 0195
[3] Patent: WO2015/27222, 2015, A2. Location in patent: Paragraph 0216
[4] Patent: US2018/208604, 2018, A1. Location in patent: Paragraph 0484-0485

956100-62-2
956100-63-3
Synthesis of 8-BROMO-2-CHLOROQUINAZOLINE from 4-Amino-8-bromo-2-chloroquinazoline

8-BROMO-2-CHLOROQUINAZOLINE Preparation Products And Raw materials

Global( 129)Suppliers
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8-BROMO-2-CHLOROQUINAZOLINE Spectrum

8-BROMO-2-CHLOROQUINAZOLINE 8-BroMo-2-chloroquinazoli... 8-Bromo-2-chloroquinazoline 97% 2-chloro-8-bromoquinazoline Quinazoline, 8-bromo-2-chloro- 956100-63-3 CHIRAL CHEMICALS