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110954-03-5

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110954-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110954-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,5 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110954-03:
(8*1)+(7*1)+(6*0)+(5*9)+(4*5)+(3*4)+(2*0)+(1*3)=95
95 % 10 = 5
So 110954-03-5 is a valid CAS Registry Number.

110954-03-5Relevant articles and documents

Synthesis of chitosan-la2o3 nanocomposite and its utility as a powerful catalyst in the synthesis of pyridines and pyrazoles

Farghaly, Thoraya A.,Hagar, Mohamed,Jaremko, Mariusz,Khalil, Khaled D.,Riyadh, Sayed M.

, (2021)

Recently, the development of nanocatalysts based on naturally occurring polysaccharides has received a lot of attention. Chitosan (CS), as a biodegradable and biocompatible polysaccharide, is considered to be an excellent template for the design of a hybr

Enaminones as building blocks in organic synthesis: A novel route to polyfunctionally substituted benzonitriles, pyridines, eneylbenzotriazoles and diazepines

Hassanien, Abu Zeid A.,Ghozlan, Said A. S.,Elnagdi, Mohamed H.

, p. 225 - 228 (2007/10/03)

An efficient synthesis of enaminones 1a-c is reported. Compounds 1a-c reacted with diethyl-3-amino-2-cyanopenten-1,5-dicarboxylate (3) to yield the benzonitriles 6. On the other hand, the reaction of 1a-c with 3-amino-2-cyano-2-pentene dinitrile (7) affor

CYCLIZATION OF 2-DICYANOMETHYLENE-1,2-DIHYDROPYRIDINE-3-CARBONITRILES WITH HYDROGEN HALIDES: A RE-EXAMINATION ON THE REGIOSELECTIVITY

Victory, Pedro,Busquets, Nuria,Borrell, Jose I.,Teixido, Jordi,Serra, Blanca,et al.

, p. 1013 - 1022 (2007/10/02)

The cyclization of the title compounds (5a-c) with HCl and HBr has been re-examined.In all cases 5-amino-7-halo-substituted 1,6-naphthyridines (11a-c and 12a-c) were formed independently of the thermal level and the hydrogen halide employed.The structures of 11a-c and 12a-c were unequivocally established by reaction with hydrazine which affforded the corresponding pyrazolonaphthyridines (14a-c).The structure of the methoxy derivatives (15a,c and 16a,c) was assigned by two-dimensional nmr studies.

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