Basic information Safety Supplier Related

5-BROMO-2-NAPHTHOIC ACID

Basic information Safety Supplier Related

5-BROMO-2-NAPHTHOIC ACID Basic information

Product Name:
5-BROMO-2-NAPHTHOIC ACID
Synonyms:
  • 5-BROMO-2-NAPHTHOIC ACID
  • 5-bromonaphthalene-2-carboxylic acid
  • 5-BroMo-2-naphthoic acid or Methyl ester
  • 5-Bromo-2-Naphthalenecarboxylic Acid 5-Bromo-2-Naphthoic Acid Or Methyl Ester
  • 2-Naphthalenecarboxylic acid, 5-bromo-
  • 2-Naphthalenecarbox
  • 5-Bromo-2-napthoicacid
  • 5-Bromo-2-Napthanoic acid
CAS:
1013-83-8
MF:
C11H7BrO2
MW:
251.08
Mol File:
1013-83-8.mol
More
Less

5-BROMO-2-NAPHTHOIC ACID Chemical Properties

Melting point:
270°C
Boiling point:
387.3±17.0 °C(Predicted)
Density 
1.5480 (rough estimate)
refractive index 
1.5845 (estimate)
storage temp. 
Sealed in dry,Room Temperature
pka
3.98±0.30(Predicted)
Appearance
Off-white to gray Solid
InChI
InChI=1S/C11H7BrO2/c12-10-3-1-2-7-6-8(11(13)14)4-5-9(7)10/h1-6H,(H,13,14)
InChIKey
QPOQPJDDJJNVRY-UHFFFAOYSA-N
SMILES
C1=C2C(C(Br)=CC=C2)=CC=C1C(O)=O
More
Less

5-BROMO-2-NAPHTHOIC ACID Usage And Synthesis

Synthesis

93-09-4

1013-83-8

General procedure for the synthesis of 5-bromo-2-naphthalenecarboxylic acid from 2-naphthalenecarboxylic acid: 1. Preparation of 3,6-iodo-1-methoxynaphthalene [CHEMMOL-00022]. 2. Preparation of 5-bromo-2-naphthalenecarboxylic acid: 2-naphthalenecarboxylic acid (50.0 g, 0.290 mol), glacial acetic acid (250 mL), bromine (15 mL, 0.291 mol), and iodine (1.3 g, 0.005 mol) were added to a flask and mixed under nitrogen protection. The mixture was heated to reflux for 35 minutes and subsequently cooled to room temperature. The resulting thick yellow mixture was stirred at room temperature for 1 hour. The mixture was filtered and the light orange solid was washed with 100 mL of filtrate. The solid was dried under vacuum at 55 °C overnight to give 55.5 g of light orange solid. 3. Slurried the above solid with 275 mL of 1N NaOH solution for 30 minutes. The solid was collected by filtration and washed with 50 mL of filtrate in three portions. The solid was air dried in a fume hood to the end of the week to yield 46.7 g of solid. 4. The solid was added to 220 mL of water, the pH was adjusted to 1.3 with the addition of concentrated hydrochloric acid (15 mL) and the mixture was stirred for 4 hours. The solid was collected by filtration and washed with 200 mL of water. The solid was dried under vacuum at 50 °C to give 37.6 g of the intermediate 5-bromo-2-naphthalenecarboxylic acid as white crystals (HPLC purity: 90%, containing 9% 2-naphthalenecarboxylic acid, 46% yield).

References

[1] Patent: US2008/58423, 2008, A1. Location in patent: Page/Page column 9
[2] Patent: US2004/6229, 2004, A1. Location in patent: Page/Page column 15
[3] Synthetic Communications, 2011, vol. 41, # 13, p. 2017 - 2024
[4] Journal of Medicinal Chemistry, 2004, vol. 47, # 8, p. 1893 - 1899
[5] Helvetica Chimica Acta, 1938, vol. 21, p. 62,65

5-BROMO-2-NAPHTHOIC ACIDSupplier

Chengdu Lanqingting Biotech Company Limited Gold
Tel
028-87856149; 15208320722
Email
1813129729@qq.com
Lanzhou Angeli Biochemical Technology Co., Ltd. Gold
Tel
0931-8235634 13321316780
Email
1455540579@qq.com
Chengdu Senior Pharma Technology Co.Ltd. Gold
Tel
+86-0838-2319818 +86-15982001943
Email
seniorpharma@163.com
Wuhan Naixing Optoelectronic Technology Co., Ltd. Gold
Tel
13407122362
Email
397959126@qq.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com
More
Less