97137-15-0 Usage
Uses
Used in Pharmaceutical Industry:
[4,5-DICHLORO-6-OXO-1(6H)-PYRIDAZINYL]METHYL ACETATE is used as an intermediate in the synthesis of various organic compounds, contributing to the development of new pharmaceutical products.
Used in Agrochemical Industry:
In the agrochemical industry, [4,5-DICHLORO-6-OXO-1(6H)-PYRIDAZINYL]METHYL ACETATE is utilized as a building block for the creation of compounds with potential applications in agriculture, such as pesticides or herbicides, aiming to improve crop protection and yield.
Precaution:
It is crucial to handle [4,5-DICHLORO-6-OXO-1(6H)-PYRIDAZINYL]METHYL ACETATE with care due to its potential reactivity and toxicity, ensuring safety measures are in place during its use and production.
Check Digit Verification of cas no
The CAS Registry Mumber 97137-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,3 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97137-15:
(7*9)+(6*7)+(5*1)+(4*3)+(3*7)+(2*1)+(1*5)=150
150 % 10 = 0
So 97137-15-0 is a valid CAS Registry Number.
97137-15-0Relevant academic research and scientific papers
Retro-ene reaction, VI. Functionalization of 4,5-dihalopyridazin-6-ones using 1-acetyloxymethyl-4,5-dihalopyridazin-6-ones as the 1-o, 3-n, 5-o ene- adduct
Chung, Hyun-A,Kang, Young-Jin,Kweon, Deok-Heon,Yoon, Yong-Jin
, p. 413 - 421 (2007/10/03)
Functionalization of 1-acetyloxymethyl-4,5-dihalopyridazin-6-ones via retro-ene reaction with some nucleophiles gave regioselectively only 5-halo- 4-substitutedpyridazin-6-ones.
Retro-ene reaction. II. Reaction of 4,5-dichloro-1-hydroxymethylpyridazin-6-one with alkyl halides and carboxylic acid chlorides
Kim, Sung-Kyu,Cho, Su-Dong,Kweon, Deok-Heon,Lee, Sang-Gyeong,Chung, Joo-Wha,Shin, Sung Chul,Yoon, Yong-Jin
, p. 245 - 248 (2007/10/03)
1-Alkyl-4,5-dichloropyridazin-6-ones and (4,5-dichloro-6-oxopyridazin-1-yl)methylcarboxylates were synthesized from 4,5-dichloro-1-hydroxymethylpyridazin-6-one and the corresponding alkyl halides or carboxylic acid chlorides. Also the reaction mechanisms via a fragmentation of retro-ene type are discussed.
