ChemicalBook > CAS DataBase List > 2-Chloro-5-nitrobenzonitrile

2-Chloro-5-nitrobenzonitrile

Product Name
2-Chloro-5-nitrobenzonitrile
CAS No.
16588-02-6
Chemical Name
2-Chloro-5-nitrobenzonitrile
Synonyms
2-chlor-5-nitrobenzonitril;2-chlor-5-nitrobenzonitrile;4-Chloro-3-cyanonitrobenzene;2-chloro-5-nitro-benzonitril;2-CHLORO-5-NITROBENZONITRILE;5-Nitro-2-chlorobenzonitrile;2-Chloro-5-nitrobenzenenitrile;BENZONITRILE, 2-CHLORO-5-NITRO-;4-Chloro-3-cyano-1-nitrobenzene;1-CHLORO-2-CYANO-4-NITROBENZENE
CBNumber
CB5395246
Molecular Formula
C7H3ClN2O2
Formula Weight
182.56
MOL File
16588-02-6.mol
More
Less

2-Chloro-5-nitrobenzonitrile Property

Melting point:
105-107 °C (lit.)
Boiling point:
122 °C / 0.6mmHg
Density 
1.6133 (rough estimate)
refractive index 
1.5557 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Orange to Green
BRN 
1818642
InChI
InChI=1S/C7H3ClN2O2/c8-7-2-1-6(10(11)12)3-5(7)4-9/h1-3H
InChIKey
ZGILLTVEEBNDOB-UHFFFAOYSA-N
SMILES
C(#N)C1=CC([N+]([O-])=O)=CC=C1Cl
CAS DataBase Reference
16588-02-6(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xn,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-37/39-36
RIDADR 
3276
WGK Germany 
3
RTECS 
DI3040000
HazardClass 
IRRITANT
HS Code 
29269090
More
Less

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.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
135712
Product name
2-Chloro-5-nitrobenzonitrile
Purity
99%
Packaging
25g
Price
$113
Updated
2025/07/31
Sigma-Aldrich
Product number
135712
Product name
2-Chloro-5-nitrobenzonitrile
Purity
99%
Packaging
100g
Price
$272
Updated
2023/01/07
TCI Chemical
Product number
C2026
Product name
2-Chloro-5-nitrobenzonitrile
Purity
>98.0%(GC)
Packaging
5g
Price
$42
Updated
2025/07/31
TCI Chemical
Product number
C2026
Product name
2-Chloro-5-nitrobenzonitrile
Purity
>98.0%(GC)
Packaging
25g
Price
$167
Updated
2025/07/31
TRC
Product number
C596660
Product name
2-Chloro-5-nitrobenzonitrile
Packaging
5g
Price
$60
Updated
2021/12/16
More
Less

2-Chloro-5-nitrobenzonitrile Chemical Properties,Usage,Production

Chemical Properties

LIGHT YELLOW CRYSTALLINE POWDER. 2-Chloro-5-nitrobenzonitrile [16588-02-6], 1-chloro-2-cyano-4-nitrobenzene, Mr 182.57, mp 108 – 109℃, forms yellow needle-shaped crystals. The chlorine atom ortho to the nitrile group is prone to a range of nucleophilic substitution reactions, of which that with ammonia has achieved industrial importance. The nitrile is produced by nitration of 2-chlorobenzonitrile (see above) at 0 ℃.

Uses

2-Chloro-5-nitrobenzonitrile was used in online detection of rat glutathione S-transferase P1-specific inhibitors by high-resolution screening technology.

General Description

2-Chloro-5-nitrobenzonitrile effectively conjugates with rat glutathione S-transferase (GST) isoenzymes and is an alternative model substrate in GST-research.

Synthesis

873-32-5

16588-02-6

100-47-0

In one embodiment of the present invention, a medium concentration of sulfuric acid solution and a medium concentration of nitric acid solution are accurately metered in proportion to each other in an acid mixing kettle. After mixing, the mixed acid is transferred to the metering tank and supplemented with an appropriate amount of nitric acid to ensure the required acidity for the reaction. Subsequently, the reaction was initiated by slowly adding 654 kg of o-chlorobenzonitrile to the nitrification reactor through the metering tank. The nitrification reaction temperature was controlled between 11 °C and 60 °C, and the reaction mixture was kept stirred in this temperature range for 1 h to ensure that the reaction proceeded adequately. The reaction process is shown in Figure 1. The specific feed amounts of the raw materials and their quality standards are detailed in Table 2. 30 kg of sulfuric acid at a concentration of 90% and 30 kg of nitric acid at a concentration of 90% were used as catalysts in the reaction system, and the amount of phthalonitrile fed was 564 kg. The composition of the reaction products was analyzed in Table 3, in which the content of 2-chloro-5-nitrobenzonitrile was 97.95%, the content of hexanitrobenzene was 1.28%, and the content of benzonitrile was 0.17%.

References

[1] Patent: CN105859581, 2016, A. Location in patent: Paragraph 4; 5

2-Chloro-5-nitrobenzonitrile Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

2-Chloro-5-nitrobenzonitrile Suppliers

Shandong Yizhi Medical Technology Co., LTD
Tel
13287715206 15508629772
Email
2786175817@qq.com
Country
China
ProdList
65
Advantage
58
Tianshui YiYao Chemical Co., Ltd.
Tel
0938-0938-8493022 1685585981;15379872136
Email
xiaoshi079@163.com
Country
China
ProdList
2018
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TAIYUAN RHF CO.,LTD.
Tel
+86 351 7031519
Fax
+86 351 7031519
Email
sales@RHFChem.com
Country
China
ProdList
2338
Advantage
56
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
Advantage
56
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9310
Advantage
66
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
More
Less

View Lastest Price from 2-Chloro-5-nitrobenzonitrile manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
2-Chloro-5-nitrobenzonitrile 16588-02-6
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2025-09-11
Shaanxi Dideu New Materials Co. Ltd
Product
2-Chloro-5-nitrobenzonitrile 16588-02-6
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
10000KGS
Release date
2025-05-20
YANGZHOU SHUANGDING CHEM CO., LTD
Product
2-Chloro-5-nitrobenzonitrile 16588-02-6
Price
US $0.00/Kg/Drum
Min. Order
100KG
Purity
99%
Supply Ability
100 tons/year
Release date
2020-08-11

16588-02-6, 2-Chloro-5-nitrobenzonitrileRelated Search:


  • 2-chlor-5-nitrobenzonitril
  • 1-butylsulfonyl-3-(4-chlorophenyl)urea
  • 4-Chloro-3-cyanonitrobenzene
  • 2-chloro-5-nitrophenyl-carbonitrile
  • 2-Chloro-5-nitrobenzonitrile, 98.5%
  • 2-chloro-5-nitro-benzonitril
  • 2-Chloro-5-nitrophenylcarbonitrle
  • 2-CHLORO-5-NITROBENZONITRILE
  • 2-chlor-5-nitrobenzonitrile
  • 4-Chloro-3-cyano-1-nitrobenzene
  • BENZONITRILE, 2-CHLORO-5-NITRO-
  • 1-CHLORO-2-CYANO-4-NITROBENZENE
  • 2-Chloro-5-nitrobenzenenitrile
  • 5-Nitro-2-chlorobenzonitrile
  • 2-Chloro-5-nitrobenzonitrile,99%
  • 2-Chloro-5-nitrobenzonitrile &gt
  • 2-Chloro-5-nitrobenzonitrile ISO 9001:2015 REACH
  • 16588-02-6
  • C7H3N2O2Cl
  • C7H3ClN2O2
  • C6 to C7
  • Building Blocks
  • Cyanides/Nitriles
  • Organic Building Blocks
  • Nitrogen Compounds
  • API Intermediate
  • blocks
  • Carboxes
  • NitroCompounds
  • Aromatic Nitriles
  • C6 to C7
  • Cyanides/Nitriles
  • Nitrogen Compounds