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750514-42-2

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750514-42-2 Usage

Description

2,4-Imidazolidinedione, 5-(2-chloroethyl)is a white crystalline solid with the molecular formula C6H10ClN3O2. It is a derivative of imidazolidine-2,4-dione and contains a chloroethyl group. This chemical compound is insoluble in water and is used as a pharmaceutical intermediate in the synthesis of various drugs.

Uses

Used in Pharmaceutical Industry:
2,4-Imidazolidinedione, 5-(2-chloroethyl)is used as a pharmaceutical intermediate for the synthesis of anticancer and antiviral drugs. Its chloroethyl group makes it a useful building block in the development of these medications.
Used in Agricultural Chemicals Production:
2,4-Imidazolidinedione, 5-(2-chloroethyl)is also used in the production of agricultural chemicals, where it serves as an important building block for various organic compounds.
Used in Neurological Disorder Treatment:
2,4-Imidazolidinedione, 5-(2-chloroethyl)has been found to have potential use in the treatment of certain neurological disorders, although further research is likely needed to fully understand its applications in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 750514-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,0,5,1 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 750514-42:
(8*7)+(7*5)+(6*0)+(5*5)+(4*1)+(3*4)+(2*4)+(1*2)=142
142 % 10 = 2
So 750514-42-2 is a valid CAS Registry Number.

750514-42-2Downstream Products

750514-42-2Relevant articles and documents

Method for preparing chlorinated hydantoin derivatives

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Paragraph 0029-0052, (2021/04/21)

The present invention relates to a process for preparing chlorohydantoin derivatives of formula (I). A compound of formula (I) is obtained by reacting a compound of formula (II) or a salt thereof, an enantiomer or a mixture of enantiomers in all proportions with hydrogen chloride or a hydrogen chloride solution. When the chlorohydantoin derivative is used for preparing glufosinate-ammonium, the problems of high cost, low efficiency and the like in the prior art can be solved, and the preparation method has the advantage of cost.

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