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893642-04-1

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893642-04-1 Usage

Chemical Class

Propargyl alcohol derivative

Functional Groups

Trifluoromethoxyphenyl group attached to propargyl moiety

Applications

Building block for synthesis of pharmaceuticals and agrochemicals
Versatile reagent in organic synthesis
Valuable tool in medicinal and material science research

Check Digit Verification of cas no

The CAS Registry Mumber 893642-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,6,4 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 893642-04:
(8*8)+(7*9)+(6*3)+(5*6)+(4*4)+(3*2)+(2*0)+(1*4)=201
201 % 10 = 1
So 893642-04-1 is a valid CAS Registry Number.

893642-04-1Relevant articles and documents

Design and synthesis of novel xanthine derivatives as potent and selective A2B adenosine receptor antagonists for the treatment of chronic inflammatory airway diseases

Basu, Sujay,Barawkar, Dinesh A.,Ramdas, Vidya,Patel, Meena,Waman, Yogesh,Panmand, Anil,Kumar, Santosh,Thorat, Sachin,Naykodi, Minakshi,Goswami, Arnab,Reddy, B. Srinivasa,Prasad, Vandna,Chaturvedi, Sandhya,Quraishi, Azfar,Menon, Suraj,Paliwal, Shalini,Kulkarni, Abhay,Karande, Vikas,Ghosh, Indraneel,Mustafa, Syed,De, Siddhartha,Jain, Vaibhav,Banerjee, Ena Ray,Rouduri, Sreekanth R.,Palle, Venkata P.,Chugh, Anita,Mookhtiar, Kasim A.

, p. 218 - 229 (2017/04/19)

Adenosine induces bronchial hyperresponsiveness and inflammation in asthmatics through activation of A2B adenosine receptor (A2BAdoR). Selective antagonists have been shown to attenuate airway reactivity and improve inflammatory cond

Chemoproteomics-Enabled Discovery of a Potent and Selective Inhibitor of the DNA Repair Protein MGMT

Wang, Chao,Abegg, Daniel,Hoch, Dominic G.,Adibekian, Alexander

supporting information, p. 2911 - 2915 (2016/02/27)

We present a novel chemical scaffold for cysteine-reactive covalent inhibitors. Chloromethyl triazoles (CMTs) are readily accessed in only two chemical steps, thus enabling the rapid optimization of the pharmacological properties of these inhibitors. We d

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