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4-chloro-1-naphthalenecarboxylic acid

Product Name
4-chloro-1-naphthalenecarboxylic acid
CAS No.
1013-04-3
Chemical Name
4-chloro-1-naphthalenecarboxylic acid
Synonyms
4-Chloro-1-naphthoic acid;4-Chloro-1-naphthoic acid, 98%;4-chloro-1-phthalenecarboxylic acid;4-Chloro-1-napthalenecarboxylic Acid;4-chloro-1-naphthalenecarboxylic acid;1-Naphthalenecarboxylic acid, 4-chloro-
CBNumber
CB72596780
Molecular Formula
C11H7ClO2
Formula Weight
206.63
MOL File
1013-04-3.mol
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4-chloro-1-naphthalenecarboxylic acid Property

Melting point:
223-224 °C
Boiling point:
398.5±15.0 °C(Predicted)
Density 
1.395±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly, Heated)
form 
Solid
pka
3.48±0.10(Predicted)
color 
Pale Yellow to Light Beige
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C370940
Product name
4-Chloro-1-napthalenecarboxylicAcid
Packaging
1g
Price
$110
Updated
2021/12/16
AK Scientific
Product number
0365AA
Product name
4-Chloro-1-naphthoicacid
Packaging
100mg
Price
$109
Updated
2021/12/16
Chemenu
Product number
CM105225
Product name
4-chloronaphthalene-1-carboxylicacid
Purity
98%
Packaging
1g
Price
$407
Updated
2021/12/16
Crysdot
Product number
CD12187532
Product name
4-Chloro-1-naphthoicacid
Purity
98%
Packaging
1g
Price
$431
Updated
2021/12/16
Alichem
Product number
1013043
Product name
4-Chloronaphthalene-1-carboxylicacid
Packaging
500mg
Price
$989.8
Updated
2021/12/16
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4-chloro-1-naphthalenecarboxylic acid Chemical Properties,Usage,Production

Uses

4-Chloro-1-napthalenecarboxylic Acid is used in the synthesis of naphthoyl-indoles as CB1 and CB2 receptor inhibitors.

Synthesis

16726-68-4

1013-04-3

Under nitrogen protection, 2.44 g (11.9 mmol) of 1-acetyl-4-chloronaphthalene was dissolved in 5 mL of freshly distilled pyridine, to this solution was added 3.33 g (13.1 mmol) of iodine dissolved in 15 mL of freshly distilled pyridine. The mixture was heated to reflux for 40 minutes, cooled to room temperature and diluted with ether until a brown precipitate formed. The precipitate was collected by filtration, suspended in 12 mL of 6 M aqueous sodium hydroxide solution and heated to reflux for 2 hours. After cooling, the solution was acidified with 10% hydrochloric acid and the crude 4-chloro-1-naphthalenecarboxylic acid was extracted into ether and the ether extract was washed with brine. After drying over magnesium sulfate, the solution was concentrated in vacuum. The product was dissolved in 25 ml of methanol and 5 ml of concentrated sulfuric acid was carefully added. The solution was heated to reflux for 3 hours. After cooling to room temperature, the crude ester was extracted into ether, the ether solution was washed with brine and dried (magnesium sulfate). The solution was concentrated in vacuum to give 1.66 g (63% yield) of methyl 4-chloro-1-naphthalenecarboxylate as a brown oil, which could be used without further purification. NMR hydrogen spectrum (300 MHz, deuterated chloroform) δ 3.90 (single peak, 3H), 7.38 (double peak, J = 7.8 Hz, 1H), 7.45-7.56 (multiple peaks, 2H), 7.87 (double peak, J = 8.1 Hz, 1H), 8.18 (double peak, J = 8.4 Hz, 1H), 8.93 (double peak, J = 8.1 Hz, 1H); NMR carbon spectrum (75.5 MHz, deuterated chloroform) δ52.1,124.6,124.9,125.8,126.2,127.1,128.3,129.9,130.7,132.3,137.2,166.9; GC/MS (electron bombardment) m/z (relative intensity) 220 (61), 189 (100) , 161 (48), 126 (42). A mixture of 0.25 g (1.1 mmol) of methyl 4-chloro-1-naphthalenecarboxylate and 2.10 g (37.4 mmol) of potassium hydroxide in 20 mL of water was heated to reflux for 12 h under nitrogen protection. The reaction mixture was cooled to room temperature, acidified with concentrated hydrochloric acid, and the product extracted into ether and dried (magnesium sulfate). The organic phase was concentrated in vacuum to give 0.27 g (88% yield) of 4-chloro-1-naphthalenecarboxylic acid as an off-white solid: melting point 223-224 °C (literature value 220-221 °C); NMR hydrogen spectrum (300 MHz, deuterium dimethylsulfoxide) δ 7.74-7.81 (multiple peaks, 3H), 8.11 (double peaks, J=6 Hz, 1H), 8.28- 8.31 (multiple peaks, 1H), 8.93-8.97 (multiple peaks, 1H), 13.8 (broad peaks, 1H); NMR carbon spectrum (75.5 MHz, deuterium dimethylsulfoxide) δ 124.7,126.1,126.7,127.9,128.3,129.0,130.4,130.6,132.3,135.7, 168.5.

References

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 6, p. 2067 - 2081
[2] Patent: EP1362846, 2003, A1. Location in patent: Page/Page column 50-51

4-chloro-1-naphthalenecarboxylic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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4-chloro-1-naphthalenecarboxylic acid Suppliers

J & K SCIENTIFIC LTD.
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18210857532; 18210857532
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86-10-82849933
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jkinfo@jkchemical.com
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China
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Alfa Aesar
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400-6106006
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021-67582001/03/05
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China
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Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
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025-66113011 17798518460
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(1)02557626880
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Shanghai Witofly Chemical Co.,Ltd
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Bide Pharmatech Ltd.
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+86-21-61629029
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China
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Shanghai Tombiopharma Chemical Co. Ltd.
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Nova(Shanghai) Pharmaceutical Co.,Ltd
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Shanghai GaoDao Pharmaceutical Co., Ltd.
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Shanghai Qiao Chemical Science Co., Ltd
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021-58892003
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Shijiazhuang Sdyano Fine Chemical Co., Ltd.
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0311-89250318 031166536426
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master@sjzsdyn.com
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China
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View Lastest Price from 4-chloro-1-naphthalenecarboxylic acid manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
4-chloro-1-naphthalenecarboxylic acid 1013-04-3
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
1000KG
Release date
2024-08-06
Career Henan Chemical Co
Product
4-chloro-1-naphthalenecarboxylic acid 1013-04-3
Price
US $1.00/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
100kg
Release date
2020-01-14

1013-04-3, 4-chloro-1-naphthalenecarboxylic acidRelated Search:


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