ChemicalBook >> CAS DataBase List >>2-Bromo-5-methoxybenzylamine

2-Bromo-5-methoxybenzylamine

CAS No.
887581-09-1
Chemical Name:
2-Bromo-5-methoxybenzylamine
Synonyms
2-Bromo-5-methoxybenzylamine;2-bromo-5-methxoxybenzylamine;(2-BROMO-5-METHOXYPHENYL)METHANAMINE;Benzenemethanamine,2-bromo-5-methoxy-
CBNumber:
CB9380246
Molecular Formula:
C8H10BrNO
Molecular Weight:
216.08
MDL Number:
MFCD07786684
MOL File:
887581-09-1.mol
Last updated:2026-09-12 18:56:27

2-Bromo-5-methoxybenzylamine Properties

Boiling point 291.1±25.0 °C(Predicted)
Density 1.444±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 8.49±0.10(Predicted)
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

2-Bromo-5-methoxybenzylamine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS117965 (2-Bromo-5-methoxyphenyl)methanamine 97% 887581-09-1 1g $211 2026-06-04 Buy
Activate Scientific AS117965 (2-Bromo-5-methoxyphenyl)methanamine 97% 887581-09-1 5g $660 2026-06-04 Buy
Matrix Scientific 213862 2-Bromo-5-methoxybenzylamine 887581-09-1 100.00mg $47 2026-05-18 Buy
Matrix Scientific 213862 2-Bromo-5-methoxybenzylamine 887581-09-1 250.00mg $57 2026-05-18 Buy
Matrix Scientific 213862 2-Bromo-5-methoxybenzylamine 887581-09-1 1.00g $100 2026-05-18 Buy
Product number Packaging Price Buy
AS117965 1g $211 Buy
AS117965 5g $660 Buy
213862 100.00mg $47 Buy
213862 250.00mg $57 Buy
213862 1.00g $100 Buy

2-Bromo-5-methoxybenzylamine Chemical Properties,Uses,Production

Synthesis

2-Bromo-5-methoxybenzonitrile

138642-47-4

2-BROMO-5-METHOXYBENZYLAMINE

887581-09-1

Step A: Synthesis of 1-(2-bromo-5-methoxyphenyl)methanamine 2-Bromo-5-methoxybenzonitrile (10.0 g, 47.2 mmol) was dissolved in dry tetrahydrofuran (100 mL) in a flame-dried flask and cooled in an ice bath. A solution of borane-tetrahydrofuran complex (75 mL, 75 mmol, 1.0 M) was added slowly and dropwise over 30 min. The reaction mixture was stirred overnight at room temperature and then the reaction was slowly quenched with ice water and saturated aqueous sodium carbonate solution. Tetrahydrofuran was removed by distillation under reduced pressure and the residue was extracted with ethyl acetate (EtOAc) several times (3 times). The organic layers were combined, washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography to afford the target product 1-(2-bromo-5-methoxyphenyl)methanamine as a white powder (3.65 g, 36% yield). m/z = 216.9, 219.0 for C8H10BrNO ([M+H]+) by LCMS analysis.

References

[1] Patent: US2010/190804, 2010, A1. Location in patent: Page/Page column 75-76
[2] Patent: WO2004/14384, 2004, A2. Location in patent: Page/Page column 235-236; 239

7507-86-0
887581-09-1
Synthesis of 2-Bromo-5-methoxybenzylamine from 2-Bromo-5-methoxybenzaldehyde

2-Bromo-5-methoxybenzylamine Preparation Products And Raw materials

2-Bromo-5-methoxybenzylamine Suppliers

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2-Bromo-5-methoxybenzylamine Spectrum

(2-BROMO-5-METHOXYPHENYL)METHANAMINE Benzenemethanamine,2-bromo-5-methoxy- 2-bromo-5-methxoxybenzylamine 2-Bromo-5-methoxybenzylamine 887581-09-1 Anilines, Aromatic Amines and Nitro Compounds