NSC45356

NSC45356 Suppliers list
Company Name: Shaanxi Dideu Medichem Co. Ltd
Tel: +86-029-81138252 +86-173 9270 1263
Email: 1057@dideu.com
Products Intro: Product Name:1,3,4-oxadiazol-2-amine
CAS:3775-60-8
Purity:99% Package:1KG;1USD
Company Name: Frapp's ChemicalNFTZ Co., Ltd.
Tel: +86 (576) 8169-6106
Email: sales@frappschem.com
Products Intro: Product Name:1,3,4-oxadiazol-2-amine
CAS:3775-60-8
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:3775-60-8
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: Accela ChemBio Inc.
Tel: +1-858-6993322
Email: info@accelachem.com
Products Intro: Product Name:2-Amino-1,3,4-oxadiazole
CAS:3775-60-8
Purity:>=95% Package:0.1g;0.25g;1g;5g;10g;25g
Company Name: Jurong Coupling Biotechnology Co., Ltd.
Tel: 13656108824
Email: coupling278191416@hotmail.com
Products Intro: Product Name:NSC45356
CAS:3775-60-8
Purity:0.98 Package:5KG;1KG

NSC45356 manufacturers

  • NSC45356
  • NSC45356 pictures
  • $9.80 / 1.79999995231628KG
  • 2020-01-15
  • CAS:3775-60-8
  • Min. Order: 1g
  • Purity: ≥99%
  • Supply Ability: 100kg
NSC45356 Basic information
Product Name:NSC45356
Synonyms:NSC45356;1,3,4-oxadiazol-2-amine;2-Amino-1,3,4-oxadiazole;1,3,4-oxadiazole-2-amine;1,3,4-Oxadiazol-2-amine - [X94278]
CAS:3775-60-8
MF:C2H3N3O
MW:85.06
EINECS:
Product Categories:
Mol File:3775-60-8.mol
NSC45356 Structure
NSC45356 Chemical Properties
Melting point 156 °C
Boiling point 205.6±23.0 °C(Predicted)
density 1.395±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka-0.75±0.10(Predicted)
AppearanceWhite to yellow Solid
Safety Information
HS Code 2934999090
MSDS Information
NSC45356 Usage And Synthesis
Synthesis
Cyanogen bromide

506-68-3

Formylhydrazine

624-84-0

NSC45356

3775-60-8

Under ice bath cooling and stirring conditions, 1.0 mL (16.65 mmol) of formylhydrazine was dissolved in 10 mL of methanol, and 1.76 g (16.62 mmol) of cyanogen bromide was added slowly and dropwise to a 10 mL methanol solution. The reaction mixture was kept at 5°C and the reaction was stirred. Over 1 hour and 30 minutes, 1.82 g (21.6 mmol) of sodium bicarbonate was added to the reaction mixture. After continuing stirring at the same temperature for 15 min, the reaction mixture was allowed to warm up naturally to room temperature and stirred continuously for 22 hrs. Upon completion of the reaction, the insoluble material was removed by filtration and the solvent was subsequently removed by distillation to give 3.12 g of light pink solid. The solid was dissolved in acetonitrile and again filtered to remove insoluble matter and the solvent was removed by distillation from the filtrate. Finally, the resulting solid was washed with ethyl ether to give 0.80 g of the target product 1,3,4-oxadiazol-2-amine as a light reddish white solid.

References[1] Patent: US2883391, 1957,
[2] Patent: JP2017/25054, 2017, A. Location in patent: Paragraph 0224
[3] Patent: JP2018/76298, 2018, A. Location in patent: Paragraph 0196
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