10520-34-0 Usage
Uses
Used in Pharmaceutical Industry:
(methylamino)[(propan-2-ylideneamino)oxy]methanone is used as an intermediate for the synthesis of various pharmaceutical compounds due to its versatility and ability to be modified into a wide range of different compounds.
Used in Agrochemical Industry:
(methylamino)[(propan-2-ylideneamino)oxy]methanone is used as an intermediate for the production of various agrochemicals, contributing to its stability and low toxicity, which are desirable properties for compounds used in the agricultural sector.
Used in Organic Chemistry Research:
(methylamino)[(propan-2-ylideneamino)oxy]methanone is used as a building block in organic chemistry research, allowing scientists to explore new reactions and synthesize novel compounds due to its unique structure containing both amino and oxime functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 10520-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10520-34:
(7*1)+(6*0)+(5*5)+(4*2)+(3*0)+(2*3)+(1*4)=50
50 % 10 = 0
So 10520-34-0 is a valid CAS Registry Number.
10520-34-0Relevant articles and documents
Cyclopropenone Oximes: Preparation and Reaction with Isocyanates
Yoshida, Hiroshi,Ohtsuka, Hideki,Yoshida, Keisuke,Totani, Yoshiyuki,Ogata, Tsuyoshi,Matsumoto, Kiyoshi
, p. 4347 - 4352 (2007/10/02)
2,3-Diphenyl-, 2-methyl-3-phenyl-, and 2-methyl-3-(4-methylphenyl)cyclopropenone oxime hydrochlorides (3) were prepared in good yields from the corresponding cyclopropenones and hydroxylamine hydrochloride in methanol.The salts 3 reacted with alkyl and aryl isocyanates in the presence of triethylamine to afford 1 : 2 addition products 4,6-diazaspirohexenones in moderate yields.In contrast, acetone, acetophenone, and cyclohexanone oximes reacted with twice excess of methyl isocyanates to give linear 1 : 1 addition products and benzophenone oxime yielded only 1 : 1 addition product.
