2-Chlorobenzonitrile
- Product Name
- 2-Chlorobenzonitrile
- CAS No.
- 873-32-5
- Chemical Name
- 2-Chlorobenzonitrile
- Synonyms
- OCBN;O-CHLOROBENZONITRILE;2-Chlorobenzon;orobenzonitriL;O-chloronitrile;ISOLEUCINE, L-(P);o-Chlorbenzonitril;2-Chlorbenzonitril;o-Chlorotolunitrile;2-chloro-benzonitril
- CBNumber
- CB6484338
- Molecular Formula
- C7H4ClN
- Formula Weight
- 137.57
- MOL File
- 873-32-5.mol
2-Chlorobenzonitrile Property
- Melting point:
- 43-46 °C(lit.)
- Boiling point:
- 232 °C(lit.)
- Density
- 1,18 g/cm3
- refractive index
- 1.4530 (estimate)
- Flash point:
- 227 °F
- storage temp.
- Store below +30°C.
- solubility
- 1g/l
- form
- Crystalline Solid
- color
- White to very slightly yellow
- BRN
- 1363916
- Exposure limits
- NIOSH: IDLH 25 mg/m3
- InChIKey
- NHWQMJMIYICNBP-UHFFFAOYSA-N
- CAS DataBase Reference
- 873-32-5(CAS DataBase Reference)
- NIST Chemistry Reference
- 2-Chlorobenzoic acid nitrile(873-32-5)
- EPA Substance Registry System
- Benzonitrile, 2-chloro- (873-32-5)
Safety
- Hazard Codes
- Xn,Xi
- Risk Statements
- 21/22-36-21/22/23
- Safety Statements
- 23
- RIDADR
- 3439
- WGK Germany
- 2
- RTECS
- DI2625000
- Hazard Note
- Harmful/Irritant
- TSCA
- Yes
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 29269095
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H302Harmful if swallowed
H311Toxic in contact with skin
H319Causes serious eye irritation
H412Harmful to aquatic life with long lasting effects
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P273Avoid release to the environment.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
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
- C24795
- Product name
- 2-Chlorobenzonitrile
- Purity
- 98%
- Packaging
- 100g
- Price
- $70.8
- Updated
- 2024/03/01
- Product number
- C1130
- Product name
- 2-Chlorobenzonitrile
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $28
- Updated
- 2024/03/01
- Product number
- C1130
- Product name
- 2-Chlorobenzonitrile
- Purity
- >98.0%(GC)
- Packaging
- 500g
- Price
- $134
- Updated
- 2024/03/01
- Product number
- B20451
- Product name
- 2-Chlorobenzonitrile, 98%
- Packaging
- 250g
- Price
- $55.65
- Updated
- 2024/03/01
- Product number
- B20451
- Product name
- 2-Chlorobenzonitrile, 98%
- Packaging
- 1000g
- Price
- $147.65
- Updated
- 2024/03/01
2-Chlorobenzonitrile Chemical Properties,Usage,Production
Chemical Properties
white to light yellow crystal powder. 2-Chlorobenzonitrile [873-32-5], 2-chloro1-cyanobenzene, Mr 137.57, mp 44.8℃, bp (101.3 kPa) 232℃, bp (1.6 kPa) 111.5℃, forms colorless crystals that readily sublime. The crystals are readily soluble in organic solvents, only sparingly soluble in water, and steam volatile.
Uses
Intermediate for the synthesis of agrochemicals, pharmaceuticals and chemical intermediates. 2-Chlorobenzonitrile is mainly used in the synthesis of dye intermediates 2-cyano-4-nitroaniline, and in the pharmaceutical industry for the synthesis of new anti-malarial drugs such as nitroquine.
Uses
2-Chlorobenzonitrile is an activated aryl chloride that is commonly used in reactions that involve the Palladium-catalyzed direct arylation of heteroaromatics (e.g. 3-aminopicolinic acid [A627800]). 2-Chlorobenzonitrile and its substituted derivatives (e.g. 2,3-dichloro-6-nitrobenzonitrile [2112-22-3]) also have potential anti-inflammatory properties.
Preparation
2-chlorobenzonitrile is obtained by the reaction of o-chlorobenzoic acid and urea: o-chlorobenzoic acid, sulfamic acid and urea are mixed and heated to about 140℃ and melted, then reacted vigorously under stirring, and a large amount of gas is released, and the temperature automatically rises to 220-230℃ for 2h. Then it is cooled to below 15℃, filtered, and the solids obtained are washed with 3% ammonia and water to neutral, then dried and the finished products are obtained.
Flammability and Explosibility
Not classified
Safety Profile
Poison by intraperitoneal route. Moderately toxic by ingestion. An eye irritant. When heated to decomposition or on contact with water, steam, acid, or acid fumes it emits toxic fumes of Cland CN-. See also NITRILES.
Synthesis
This embodiment includes the following steps: Step 1. Add 14.3g (0.1mol) o-chlorobenzyl alcohol, 3.7g copper-manganese composite catalyst and 1.6g (0.01mol) 2,2,6,6-tetramethylpiperidine oxide into the reaction kettle, Then add an alcohol-water mixed solution made by mixing 33 mL of ethanol and 66 mL of deionized water, Pour ammonia gas into the reactor until the ammonia gas pressure in the reactor is 0.2MPa, and then close the ammonia gas inlet valve. Continue to feed oxygen into the reaction kettle to a pressure of 0.4MPa, and then continue to supply oxygen at this pressure; The copper-manganese composite catalyst consists of 1.7 g (0.01 mol) copper chloride dihydrate and 2.0 g (0.01 mol) manganese chloride tetrahydrate; Turn on the magnetic stirring device in the reaction kettle, and at the same time heat it to the temperature of the system in the reaction kettle at 40??C to perform ammonia oxidation reaction for 4 hours After the reaction is over, the pressure of the reactor is relieved, the product system after the ammoxidation reaction is cooled to 5??C, and 14.0 g of off-white needle-like solids are obtained by suction filtration, namely crude o-chlorobenzonitrile; Step 2: Using 28 mL of alcohol-water mixed solution to recrystallize 14.0 g of the crude o-chlorobenzonitrile obtained in step 1, to obtain white needle-like crystals, namely o-chlorobenzonitrile; The alcohol-water mixed solution is formed by mixing ethanol and deionized water in a volume ratio of 1:2. The o-chlorobenzonitrile prepared in this example was dried and weighed 13.3g; after calculation, The yield of the o-chlorobenzonitrile prepared in this example was 97.1%, and the mass purity of the o-chlorobenzonitrile prepared in the example was 97.5% as determined by gas chromatography.
Purification Methods
Crystallise the nitrile to a constant melting point from *benzene/pet ether (b 40-60o). [Beilstein 9 IV 965.]
2-Chlorobenzonitrile Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2-Chlorobenzonitrile manufacturers
- Product
- 2-Chlorobenzonitrile 873-32-5
- Price
- US $1000.00-400.00/ton
- Min. Order
- 1ton
- Purity
- 99%
- Supply Ability
- 5000
- Release date
- 2024-08-12
- Product
- 2-Chlorobenzonitrile 873-32-5
- Price
- US $120.00/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- 20ton
- Release date
- 2024-05-11
- Product
- 2-Chlorobenzonitrile 873-32-5
- Price
- US $56.00/KG
- Min. Order
- 25KG
- Purity
- 98%
- Supply Ability
- 1-20mt
- Release date
- 2021-06-04