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59591-90-1

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59591-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59591-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,9 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59591-90:
(7*5)+(6*9)+(5*5)+(4*9)+(3*1)+(2*9)+(1*0)=171
171 % 10 = 1
So 59591-90-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H17N3O/c1-21(2)15-10-8-13(9-11-15)12-16-18(22)20-17(19-16)14-6-4-3-5-7-14/h3-12H,1-2H3,(H,19,20,22)/b16-12+

59591-90-1Downstream Products

59591-90-1Relevant articles and documents

Enhancement for the fluorescent properties of new synthesized GFPs chromophore

Elgendy, Bahaa,Azab,Gamil, Marwa,El-Feky, Hesham H.

, p. 3717 - 3727 (2021/07/10)

An alternative method for the synthesis of new GFP chromophore analogous that possess good photo physical properties which can be used as efficient biomarkers. These compounds have low fluorescence most probably due to their Z–E photo isomerization. These

Efficient microwave-assisted synthesis and antioxidant activity of 4-arylidene-2-phenyl-1H-imidazol-5(4H)-ones

Shi, Feng,Zeng, Xiao-Ning,Wu, Fei-Yue,Yan, Shu,Zheng, Wei-Fa,Tu, Shu-Jiang

experimental part, p. 59 - 63 (2012/04/23)

The efficient synthesis of 4-arylidene-2-phenyl-1H-imidazol-5(4H)-ones was achieved via microwaveassisted reactions of 4-arylmethylene-2-phenyloxazol-5(4H) -ones with urea in glycol. This approach provides a facile shortcut for the synthesis of this type

A Convenient Synthesis of Unsaturated 2,4-Disubstituted 2-Imidazolin-5-ones

Devasia, Ganapathiplackal M.,Shafi, P. Mohamed

, p. 657 - 660 (2007/10/02)

Twenty five unsaturated 2,4-disubstituted 2-imidazolin-5-ones (IV) have been prepared in 23-71percent yields by condensing aromatic aldehydes with a mixture of ethyl chloroacetate and an aromatic amidinium chloride in the presence of sodium hydrogencarbonate.Twenty three of them have also been prepared in 62-97percent yields by this method using ethyl bromoacetate instaed of the chloroacetate.Further, two unsaturated 2-imidazolin-5-ones (IV) have been prepared by these two methods using cyclohexanone (yields 33percent each) and cinnamaldehyde (yields 0 and 18percent) instead of the aromatic aldehydes.

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