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117550-35-3

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117550-35-3 Usage

Description

(2-hydroxymethyl-phenyl)-urea is a chemical compound that consists of a urea molecule with a hydroxymethyl-phenyl group attached to it. It is known for its potential biological activities and versatile chemical structure, making it a valuable compound for research and applications in various fields.

Uses

Used in Pharmaceutical Industry:
(2-hydroxymethyl-phenyl)-urea is used as a building block for synthesizing various drugs and biologically active compounds. Its unique structure allows for the development of new pharmaceuticals with potential therapeutic benefits.
Used in Anticancer Applications:
(2-hydroxymethyl-phenyl)-urea is used as an anticancer and antiproliferative agent. It has been studied for its potential to inhibit the growth and proliferation of cancer cells, making it a promising candidate for cancer treatment.
Used in Enzyme Inhibition:
(2-hydroxymethyl-phenyl)-urea is used in inhibiting the enzyme dihydrofolate reductase. This enzyme plays a crucial role in the synthesis of DNA and RNA, and its inhibition can lead to the suppression of cancer cell growth.
Used in Agricultural Chemicals:
(2-hydroxymethyl-phenyl)-urea has been explored for its potential use in the production of herbicides and agricultural chemicals. Its chemical properties make it a candidate for developing new compounds to control the growth of unwanted plants and improve crop yields.

Check Digit Verification of cas no

The CAS Registry Mumber 117550-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 117550-35:
(8*1)+(7*1)+(6*7)+(5*5)+(4*5)+(3*0)+(2*3)+(1*5)=113
113 % 10 = 3
So 117550-35-3 is a valid CAS Registry Number.

117550-35-3Downstream Products

117550-35-3Relevant articles and documents

Synthesis of 2-amino-4H-3,1-benzoxazines from diphenyl cyanocarbonimidate. Facile replacement of the N-cyanoimine function by nitrogen nucleophiles

Garratt,Hobbs,Wrigglesworth

, p. 829 - 834 (2007/10/02)

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