23695-15-0 Usage
Uses
Used in Polymer Production:
2-METHYL-3-NITROPHENYL ISOCYANATE is used as a monomer in the production of various polymers. Its high reactivity allows it to form strong covalent bonds with other molecules, resulting in the creation of polymers with unique properties.
Used in Pharmaceutical Industry:
2-METHYL-3-NITROPHENYL ISOCYANATE is used as a chemical intermediate in the synthesis of pharmaceuticals. Its reactive nature enables it to be incorporated into the structure of various drug molecules, potentially enhancing their therapeutic effects.
Used in Research and Development:
2-METHYL-3-NITROPHENYL ISOCYANATE is used as a research chemical in the development of new materials and compounds. Its unique properties and reactivity make it a valuable tool for scientists and researchers in various fields, including chemistry, materials science, and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 23695-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,9 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23695-15:
(7*2)+(6*3)+(5*6)+(4*9)+(3*5)+(2*1)+(1*5)=120
120 % 10 = 0
So 23695-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O3/c1-6-7(9-5-11)3-2-4-8(6)10(12)13/h2-4H,1H3
23695-15-0Relevant articles and documents
MAYTANSINOID DERIVATIVES, CONJUGATES THEREOF, AND METHODS OF USE
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Paragraph 0781; 0782; 0781; 0790, (2017/09/20)
Provided herein are maytansinoid compounds, derivatives thereof, conjugates thereof, and methods of treating or preventing proliferative diseases with the same.
A simple and efficient synthesis of diaryl ureas with reduction of the intermediate isocyanate by triethylamine
Zhou, Shuguang,Yao, Ting,Yi, Jicheng,Li, Dashuai,Xiong, Jing
, p. 315 - 319 (2013/07/27)
Thirty symmetrical diaryl urea derivatives were synthesised in moderate to excellent yields from arylamine and triphosgene with triethylamine as a reducing agent for the intermediate, isocyanate. It was significant that part of the products could be collected in almost quantitative yield without column chromatography. The procedure under mild reaction conditions was tolerant of a wide range of functional groups. The structures of the compounds were determined by NMR, MS and X-ray crystallographic analyses.
