183695
2′-Bromoacetophenone
99%
Manufacturer: Sigma Aldrich
CAS Number: 2142-69-0
Synonym(S): 1-Acetyl-2-bromobenzene
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 183695-5-G | In Stock | ₹ 4,481.55 |
| 25 G | 183695-25-G | In Stock | ₹ 10,792.53 |
183695 - 5 G
In Stock
Quantity
1
Base Price: ₹ 4,481.55
GST (18%): ₹ 806.679
Total Price: ₹ 5,288.229
Quality Level
100
Assay
99%
form
liquid
refractive index
n20/D 1.568 (lit.)
density
1.476 g/mL at 25 °C (lit.)
SMILES string
CC(=O)c1ccccc1Br
InChI
1S/C8H7BrO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,1H3
InChI key
PIMNFNXBTGPCIL-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
Sigma Aldrich Fine Chemicals Biosciences 2'-Bromoacetophenone 99% | 2142-69-0 | MFCD00000067 | 25G | -- | ₹ 15,045.45 | ||
Sigma Aldrich Fine Chemicals Biosciences 2′-Bromoacetophenone | 2142-69-0 | MFCD00000067 | 5g | -- | ₹ 7,146.70 | ||
eMolecules 2'-Bromoacetophenone | 2142-69-0 | MFCD00000067 | 25g | -- | ₹ 4,426.86 | ||
2'-Bromoacetophenone | -- | ₹ 890.00 - ₹ 62,834.00 |
Description
- General description: 2′-Bromoacetophenone (2-Bromoacetophenone) undergoes enantioselective addition reaction with phenylacetylene catalyzed by chiral camphorsulfonamide[1]. It reacts with aliphatic primary amines in the presence of palladium catalyst to afford 3-methyleneisoindolin-1-ones[2].
- Application: 2′-Bromoacetophenone (2-Bromoacetophenone) was used in the synthesis of novel series of non-condensed 5,5-bicycles[3].
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves