N'-Hydroxycyclopropanecarboximidamide

N'-Hydroxycyclopropanecarboximidamide Suppliers list
Company Name: Shanghai Anmike Chemical Co. Ltd.  Gold
Tel: 微信 18019252918 18019252918
Email: sale@amkchem.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Accela ChemBio Co.,Ltd.  
Tel: 021-50795510 4000665055
Email: marketing@accelachem.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn

N'-Hydroxycyclopropanecarboximidamide manufacturers

N'-Hydroxycyclopropanecarboximidamide Basic information
Product Name:N'-Hydroxycyclopropanecarboximidamide
Synonyms:AKOS B030098;N-HYDROXYCYCLOPROPANECARBOXAMIDINE;Cyclopropanecarboximidamide, N-hydroxy- (9CI);N'-Hydroxycyclopropanecarboximideamide;Cyclopropanecarboxamide oxime;(Z)-N'-hydroxycyclopropanecarboxamidine;Cyclopropanecarboximidamide,N-hydroxy-;N'-Hydroxycyclopropanecarboximidamide
CAS:51285-13-3
MF:C4H8N2O
MW:100.12
EINECS:
Product Categories:AMIDINE;OXIME;pharmacetical
Mol File:51285-13-3.mol
N'-Hydroxycyclopropanecarboximidamide Structure
N'-Hydroxycyclopropanecarboximidamide Chemical Properties
Melting point 34-40°
Boiling point 176.0±23.0 °C(Predicted)
density 1.50±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka15.04±0.20(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C4H8N2O/c5-4(6-7)3-1-2-3/h3,7H,1-2H2,(H2,5,6)
InChIKeyOMCUPXRCMTUDHI-UHFFFAOYSA-N
SMILESC1(C(NO)=N)CC1
CAS DataBase Reference51285-13-3
Safety Information
HazardClass IRRITANT
MSDS Information
N'-Hydroxycyclopropanecarboximidamide Usage And Synthesis
UsesN''-Hydroxycyclopropanecarboximidamide
Synthesis
Cyclopropanecarbonitrile

5500-21-0

N'-Hydroxycyclopropanecarboximidamide

51285-13-3

General procedure for the synthesis of N-hydroxycyclopropanecarboxamidine from cyclopropanecarbonitrile: A mixture of cyclopropanecarbonitrile (5 g, 74.6 mmol) and hydroxylamine (50 wt% aqueous, 5.91 g, 89.5 mmol) in ethanol (15 mL) was reacted with stirring at 80 °C overnight. Upon completion of the reaction, the mixture was cooled to room temperature and the volatile solvent was subsequently removed under reduced pressure to afford the crude product N-hydroxycyclopropanecarboxamidine (7.0 g, 94% yield). The product could be directly used in the subsequent reaction without further purification. The product was analyzed by LCMS showing m/z = 101.2 [M + H]+, which was consistent with the theoretically calculated value (exact mass of C4H8N2O: 100.1).1H NMR (400 MHz, DMSO-d6) data were as follows: δ 0.54-0.60 (m, 2H), 0.61-0.66 (m, 2H), 1.28-1.36 (m, 1H) , 5.18 (bs, 2H), 8.68 (bs, 1H).

References[1] Patent: WO2012/145361, 2012, A1. Location in patent: Page/Page column 167; 168
[2] Patent: WO2011/104680, 2011, A1. Location in patent: Page/Page column 82
[3] Patent: US5464848, 1995, A
[4] Patent: US5106853, 1992, A
[5] Patent: US5124460, 1992, A
N'-Hydroxycyclopropanecarboximidamide Preparation Products And Raw materials
Raw materialsCyclopropanecarbonitrile-->Water-->Hydroxylamine-->Ethanol
Tag:N'-Hydroxycyclopropanecarboximidamide(51285-13-3) Related Product Information
N-Hydroxypropionamidine Cyclopropanecarboxamidoxime,monohydrochloride N'-hydroxycyclopropanecarboximidamide hydrochloride CYCLOPROPANECARBOXAMIDINE N'-Hydroxy-2-methylpropanimidamide N-HYDROXYBUTYRAMIDINE N'-Hydroxycyclopropanecarboximidamide