2-Naphthaleneboronic acid
description Uses Solubility Application- Product Name
- 2-Naphthaleneboronic acid
- CAS No.
- 32316-92-0
- Chemical Name
- 2-Naphthaleneboronic acid
- Synonyms
- NAPHTHALEN-1-YLBORONIC ACID;NAPHTHALEN-2-YLBORONIC ACID;2-NAPHTHYLBORONIC ACID;NAPHTHALENE-2-BORONIC ACID;NAPHTHALENE-1-BORONIC ACID;2-Naphthene;AKOS BRN-0041;AKOS BRN-0020;eneboronic Acid;RARECHEM AH PB 0126
- CBNumber
- CB1282654
- Molecular Formula
- C10H9BO2
- Formula Weight
- 171.99
- MOL File
- 32316-92-0.mol
2-Naphthaleneboronic acid Property
- Melting point:
- 269-275 °C(lit.)
- Boiling point:
- 381.9±25.0 °C(Predicted)
- Density
- 1.21±0.1 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- Water Solubility
- Slightly soluble in water
- pka
- 8.53±0.30(Predicted)
- form
- Crystalline Powder and/or Chunks
- color
- White to off-white
- BRN
- 2936449
- InChI
- InChI=1S/C10H9BO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,12-13H
- InChIKey
- KPTRDYONBVUWPD-UHFFFAOYSA-N
- SMILES
- C1=C2C(C=CC=C2)=CC=C1B(O)O
- CAS DataBase Reference
- 32316-92-0(CAS DataBase Reference)
Safety
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- TSCA
- No
- HazardClass
- IRRITANT
- HS Code
- 29319090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 480134
- Product name
- 2-Naphthylboronic acid
- Purity
- ≥95.0%
- Packaging
- 5g
- Price
- $61.77
- Updated
- 2025/07/31
- Product number
- 480134
- Product name
- 2-Naphthylboronic acid
- Purity
- ≥95.0%
- Packaging
- 25g
- Price
- $64.5
- Updated
- 2025/07/31
- Product number
- N0649
- Product name
- 2-Naphthaleneboronic Acid (contains varying amounts of Anhydride)
- Packaging
- 1g
- Price
- $20
- Updated
- 2025/07/31
- Product number
- N0649
- Product name
- 2-Naphthaleneboronic Acid (contains varying amounts of Anhydride)
- Packaging
- 5g
- Price
- $58
- Updated
- 2025/07/31
- Product number
- N0649
- Product name
- 2-Naphthaleneboronic Acid (contains varying amounts of Anhydride)
- Packaging
- 25g
- Price
- $172
- Updated
- 2025/07/31
2-Naphthaleneboronic acid Chemical Properties,Usage,Production
description
2-Naphthalene Boronic Acid is an organometallic iridium complex with applications in catalysis and Pharmaceutical manufacturing. It can be also used in the study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols.
Uses
2-Naphthaleneboronic acid is a useful research chemical for organic synthesis and other chemical processes.
Solubility
Solubility in water: slightly soluble. Other solubilities: soluble in methanol
Application
It is used to study the enantioselective rhodium-catalyzed addition reaction of arylboronic acid and 2,2,2-trifluoroacetophenone to generate chiral tertiary trifluoromethanol.
It can also be used to study the palladium-catalyzed addition reaction of arylboronic acid and nitrile to generate aryl ketones, and aromatic adverbial clauses: palladium-catalyzed addition of oxynitrile to benzofuran.
Chemical Properties
yellow crystal powde
Uses
suzuki reaction
Uses
Used in a study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols. Also employed in a study of a palladium-catalyzed addition of aryl boronic acids to nitriles providing aryl ketones and to aryloxy nitriles providing benzofurans.
Synthesis
To a two-neck 250mL round bottom flask, triisopropyl borate (3.30mL, 29.06mmol) and 3-bromoquinoline (3.00g, 14.49mmol) was dissolved in dry THF (100mL), then n-butyllithium (14.50mL of a 2M solution in hexane, 29.00mmol) was added dropwise via a dropping funnel over 1h under N2 at-78°C. After 2h, the acetone/dry ice bath was removed, and the reaction solution was allowed to warm to 0°C. The reaction was then quenched with a 2M HCl solution, and the pH value was adjusted to 7 with a solution of 2M NaHCO3. The resulting solution was extracted with ethyl acetate (EA) (3×100mL). The combined organic layers were dried with MgSO4 and evaporated to dryness. n-Hexane was then added to precipitated the product 2-Naphthaleneboronic acid as a white solid (80% yield).
2-Naphthaleneboronic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2-Naphthaleneboronic acid manufacturers
- Product
- 2-Naphthaleneboronic acid 32316-92-0
- Price
- US $999.00-666.00/ton
- Min. Order
- 1ton
- Purity
- 99%
- Supply Ability
- 5000
- Release date
- 2024-08-09
- Product
- 2-Naphthaleneboronic acid 32316-92-0
- Price
- US $10.00/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- 20 ton
- Release date
- 2024-11-18
- Product
- 2-Naphthaleneboronic acid 32316-92-0
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 1ton
- Release date
- 2022-09-28