ChemicalBook > CAS DataBase List > 2-Chloro-5-iodobenzoic acid

2-Chloro-5-iodobenzoic acid

Product Name
2-Chloro-5-iodobenzoic acid
CAS No.
19094-56-5
Chemical Name
2-Chloro-5-iodobenzoic acid
Synonyms
SOTA-011;BUTTPARK 100\01-43;Englitin Impurity 13;Chloro-5-iodobenzoicA;3-Oxetanol,9-ethynyl-;Dagliar Net Impurity 69;2-Chloro-5-iodobenoicacid;2-Chloro-5-Iodbenzoic acid;2-CHLORO-5-IODOBENZOIC ACID;2-choloro-5-iodobenzoicacid
CBNumber
CB8283498
Molecular Formula
C7H4ClIO2
Formula Weight
282.46
MOL File
19094-56-5.mol
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2-Chloro-5-iodobenzoic acid Property

Melting point:
157-161 °C (lit.)
Boiling point:
353.1±27.0 °C(Predicted)
Density 
2.077±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
2.53±0.25(Predicted)
color 
Yellow to light brown crystals or crystalline powder (light sensitive)
Sensitive 
Light Sensitive
BRN 
2254110
InChI
InChI=1S/C7H4ClIO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,(H,10,11)
InChIKey
GEBYSTBEDVQOTK-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC(I)=CC=C1Cl
CAS DataBase Reference
19094-56-5(CAS DataBase Reference)
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Safety

Hazard Codes 
T,N,Xi
Risk Statements 
25-41-50/53
Safety Statements 
26-39-45-60-61
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
Hazard Note 
Irritant
PackingGroup 
III
HS Code 
29163990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H318Causes serious eye damage

H400Very toxic to aquatic life

Precautionary statements

P273Avoid release to the environment.

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

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
631736
Product name
2-Chloro-5-iodobenzoic acid
Purity
97%
Packaging
25g
Price
$79.8
Updated
2025/07/31
Sigma-Aldrich
Product number
631736
Product name
2-Chloro-5-iodobenzoic acid
Purity
97%
Packaging
5g
Price
$27
Updated
2023/06/20
TCI Chemical
Product number
C2168
Product name
2-Chloro-5-iodobenzoic Acid
Purity
>97.0%(GC)(T)
Packaging
5g
Price
$69
Updated
2025/07/31
TCI Chemical
Product number
C2168
Product name
2-Chloro-5-iodobenzoic Acid
Purity
>97.0%(GC)(T)
Packaging
25g
Price
$206
Updated
2025/07/31
TRC
Product number
C367570
Product name
2-Chloro-5-iodobenzoic acid
Packaging
25g
Price
$95
Updated
2021/12/16
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2-Chloro-5-iodobenzoic acid Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystal powder

Uses

2-Chloro-5-iodobenzoic Acid is a useful synthetic intermediate. It is used to prepare metabotropic glutamate receptor subtype-??2 (mGluR2) positive allosteric modulator (PAM). It is also used to synthesize quinolone carboxylic acids as cell-permeable inhibitors of protein tyrosine phosphatase.

Synthesis

89-54-3

19094-56-5

The general procedure for the synthesis of 2-chloro-5-iodobenzoic acid from 5-amino-2-chlorobenzoic acid was as follows: 123 g of 2-chloro-5-aminobenzoic acid was added to 2000 g of 20% aqueous sulfuric acid solution, and the temperature of the reaction was maintained at 0 to 10 °C. An aqueous sodium nitrite solution (51 g sodium nitrite dissolved in 200 g water) was prepared and added drop by drop to the reaction system, and the progress of the reaction was monitored by TLC (unfolding agent ratio of petroleum ether/ethyl acetate = 1:3) during the reaction. Upon completion of the reaction, 1.2 g of urea was added and cooled to 0 °C with stirring, potassium iodide solution (130 g KI dissolved in 500 g of water) was quickly added and stirring was continued until no bubbles were produced and then stirred for 30 min. The reaction mixture was filtered and washed with 200 g of water to give a brown solid. The solid was dissolved in 400 g of ethyl acetate and washed sequentially with 300 mL of 1N hydrochloric acid, 300 mL of 10% sodium bisulfite solution and 400 mL of saturated brine, and the organic phase was dried with magnesium sulfate. After drying, the crude product was obtained by concentration under reduced pressure at 50 °C. The crude product was dissolved in 400 mL of toluene and heated at 80 °C for 1 hour, then cooled to 0-5 °C for 1 hour for crystallization. Finally, it was dried under reduced pressure at 50 °C to give 191 g of 2-chloro-5-iodobenzoic acid as a pale yellow solid with 99.6% purity and 93.7% yield.

References

[1] Patent: CN106748721, 2017, A. Location in patent: Paragraph 0031; 0032
[2] RSC Advances, 2017, vol. 7, # 86, p. 54881 - 54891

2-Chloro-5-iodobenzoic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 2-Chloro-5-iodobenzoic acid manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
2-Chloro-5-iodobenzoic acid 19094-56-5
Price
US $10.00/KG
Min. Order
100KG
Purity
99%
Supply Ability
100 mt
Release date
2024-12-02
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
2-Chloro-5-iodobenzoic acid 19094-56-5
Price
US $1000.00-400.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000
Release date
2024-08-12
Hebei Chuanghai Biotechnology Co., Ltd
Product
2-Chloro-5-iodobenzoic acid 19094-56-5
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-30

19094-56-5, 2-Chloro-5-iodobenzoic acidRelated Search:


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  • 2-Chloro-5-iodobenoicacid
  • 19094-56-5
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  • C7H4CIIO2
  • C7H4O2ClI
  • Organic Building Blocks
  • C7
  • Carbonyl Compounds
  • Carboxylic Acids
  • Building Blocks
  • C7
  • Carbonyl Compounds
  • Carboxylic Acids
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Phenylacetic acid
  • Acids & Esters
  • Chlorine Compounds
  • Iodine Compounds
  • bc0001
  • 19094-56-5