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5-Bromo-2-methoxyphenol

5-Bromo-2-methoxyphenol Structure
CAS No.
37942-01-1
Chemical Name:
5-Bromo-2-methoxyphenol
Synonyms
5-Bromoguaiacol;5-Bromoguaiacol (OH=1);5-Brom-2-methoxy-phenol;5-BROMO-2-METHOXYPHENOL;4-Bromo-2-hydroxyanisole;Phenol, 5-broMo-2-Methoxy-;5-Bromo-2-methoxyphenol >5-Bromo-2-Methoxyphenol,>98%;5-Bromo-2-methoxyphenol ,99%;3-HYDROXY-4-METHOXYBROMOBENZENE
CBNumber:
CB8762773
Molecular Formula:
C7H7BrO2
Molecular Weight:
203.03
MOL File:
37942-01-1.mol
MSDS File:
SDS
Modify Date:
2024/4/16 16:23:18

5-Bromo-2-methoxyphenol Properties

Melting point 64-70
Boiling point 150 °C / 20mmHg
Density 1.585±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
form powder to crystal
pka 9.01±0.10(Predicted)
color White to Almost white
InChIKey OLSJHVZRUFFIPL-UHFFFAOYSA-N
CAS DataBase Reference 37942-01-1(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  20/21/22-36/37/38
Safety Statements  26-36/37/39
Hazard Note  Irritant/Store Cold
HazardClass  IRRITANT
HS Code  29095000
NFPA 704
0
1 0

5-Bromo-2-methoxyphenol price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) B3342 5-Bromo-2-methoxyphenol min. 98.0 % 37942-01-1 5G ₹6700 2022-05-26 Buy
TCI Chemicals (India) B3342 5-Bromo-2-methoxyphenol min. 98.0 % 37942-01-1 25G ₹10500 2022-05-26 Buy
Product number Packaging Price Buy
B3342 5G ₹6700 Buy
B3342 25G ₹10500 Buy

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

Chemical Properties

White to off-white crystal

Uses

The 5-Bromo-2-methoxyphenol is the important intermediate of producing depressor aliskiren.

Synthesis

The 5-bromo-2-methoxyphenol is synthesized by virtue of three steps of reactions as follows: by taking o-methoxyphenol as the raw materials, performing acetylation protection on the phenolic hydroxyl by use of acetic anhydride, and then performing bromination by use of bromine under the catalysis of iron powder, and finally performing deacetylation.

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5-BROMO-2-METHOXYPHENOL 3-HYDROXY-4-METHOXYBROMOBENZENE 5-Brom-2-methoxy-phenol 5-Bromo-2-methoxyphenol ,99% 5-Bromoguaiacol (OH=1) 4-Bromo-2-hydroxyanisole Phenol, 5-broMo-2-Methoxy- 4-Bromo-2-hydroxyanisole, 5-Bromoguaiacol 5-Bromo-2-methoxyphenol > 5-Bromo-2-Methoxyphenol,>98% 5-Bromoguaiacol 37942-01-1 blocks Bromides