1-amino-2-naphthonitrile

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Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: Cool Pharm, Ltd  
Tel: 021-60455363 18019463053
Email: sales@coolpharm.com
Company Name: Shanghai SuperLan Chemcial Technique Centre  
Tel: 0-2022843681 15618226720
Email: chaolaichem@foxmail.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Suzhou Shanyang Pharmaceutical Technology Co.,  
Tel: 0512-63268889 18506119477
Email: 82169840@qq.com

1-amino-2-naphthonitrile manufacturers

1-amino-2-naphthonitrile Basic information
Product Name:1-amino-2-naphthonitrile
Synonyms:1-amino-2-naphthonitrile;2-Naphthalenecarbonitrile, 1-amino-;1-amino-2-naphthalenecarbonitrile;1-Amino-2-Cyanonaphthalene;CPD0714
CAS:3100-67-2
MF:C11H8N2
MW:168.19
EINECS:
Product Categories:
Mol File:3100-67-2.mol
1-amino-2-naphthonitrile Structure
1-amino-2-naphthonitrile Chemical Properties
Melting point 191-192 °C(Solv: water (7732-18-5); benzene (71-43-2))
Boiling point 151-152 °C(Press: 0.3 Torr)
density 1.22±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka-0.32±0.10(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
MSDS Information
1-amino-2-naphthonitrile Usage And Synthesis
Synthesis
1-Nitronaphthalene

86-57-7

Ethyl cyanoacetate

105-56-6

1-amino-2-naphthonitrile

3100-67-2

General procedure for the synthesis of 1-amino-2-cyano naphthalene from 1-nitronaphthalene and ethyl cyanoacetate: In a dry 2L reactor, 139.8 g (1.236 mol) of ethyl cyanoacetate, 29.5 g (0.453 mol) of potassium cyanide, 46.2 g (0.824 mol) of potassium hydroxide, and 920 mL of dimethylformamide were added, and dissolved with stirring at 10 °C. Stirring was continued for 20 minutes under nitrogen protection. Subsequently, the reaction mixture was heated to 60°C and the reaction was stirred for 4 hours. Upon completion of the reaction, the reaction solvent was concentrated and 600 mL of 10% aqueous sodium hydroxide solution was added and stirred under reflux conditions for 1 hour. The reaction mixture was filtered and purified by column chromatography using dichloromethane and heptane as eluents to give 50 g (yield: 60%) of the target product labeled as [Intermediate 1-a].

References[1] Patent: KR2015/111106, 2015, A. Location in patent: Paragraph 0259-0262
[2] Patent: KR2016/2328, 2016, A. Location in patent: Paragraph 0476
[3] Patent: KR2015/144120, 2015, A. Location in patent: Paragraph 0310-0313
[4] Patent: KR2018/10087, 2018, A. Location in patent: Paragraph 0578-0582
[5] Pest Management Science, 2001, vol. 57, # 7, p. 625 - 632
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