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1374753-93-1

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1374753-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374753-93-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,7,5 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1374753-93:
(9*1)+(8*3)+(7*7)+(6*4)+(5*7)+(4*5)+(3*3)+(2*9)+(1*3)=191
191 % 10 = 1
So 1374753-93-1 is a valid CAS Registry Number.

1374753-93-1Downstream Products

1374753-93-1Relevant articles and documents

MNPs-NHC6H4SO3H as high-performance catalyst for the synthesis of 1,4-diazepines containing tetrazole ring under microwave irradiation

Safaei-Ghomi, Javad,Paymard-Samani, Soleiman,Shahbazi-Alavi, Hossein

, p. 1119 - 1126 (2018)

MNPs-NHC6H4SO3H as an efficient catalyst was prepared and characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), DLS dynamic light scattering (DLS), and thermogravimetric analysis (TGA) techniques. The catalytic activity of MNPs-NHC6H4SO3H was investigated in the synthesis of 1,4-diazepines containing the tetrazole ring via a four-component reaction under microwave irradiation. The heterogeneous catalyst could be recovered easily and reused six times without significant loss of its catalytic activity. The present work demonstrates the advantages of microwave irradiation-assisted heterogeneous catalysis in the synthesis of 1,4-diazepines containing the tetrazole ring, compounds that generate great attention in many applications, particularly in medicinal chemistry and drug discovery.

A two-step synthesis of 1H-tetrazolyl-1H-1,4-benzonitriles and 1H-tetrazolyl-benzo[b ][1,4]diazepines

Shaabani, Ahmad,Mofakham, Hamid,Mousavifaraz, Sajjad

experimental part, p. 731 - 736 (2012/07/02)

A two-step synthetic protocol for the title heteroannulated diazepines has been developed. The approach includes a pseudo five-component isocyanide-based condensation reaction between diamines, ketones, isocyanides and trimethylsilyl azide and proceeds in good yields. Georg Thieme Verlag Stuttgart · New York.

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