6830-81-5 Usage
General Description
3-hydroxy-N-methylpropanamide, also known as SALTDATA: FREE, is a chemical compound with the molecular formula C4H9NO2. It is a derivative of propanamide and contains a hydroxyl group, a methyl group, and an amide functional group. 3-hydroxy-N-methylpropanamide(SALTDATA: FREE) is commonly used in pharmaceutical and chemical industries for its properties and applications. It has potential uses as a building block in the synthesis of various organic compounds and pharmaceuticals due to its reactivity and functional groups. Additionally, it may have applications in the development of new drugs and pharmaceutical formulations. However, further research and testing may be necessary to fully understand and utilize the potential benefits and applications of 3-hydroxy-N-methylpropanamide in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6830-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6830-81:
(6*6)+(5*8)+(4*3)+(3*0)+(2*8)+(1*1)=105
105 % 10 = 5
So 6830-81-5 is a valid CAS Registry Number.
6830-81-5Relevant articles and documents
Reaction of Cyclopropanamines with Hypochlorite
Vaidyanathan, Ganesan,Wilson, Joseph W.
, p. 1815 - 1820 (2007/10/02)
Ethylene was formed in 65percent yield when 1-(1-piperidino)cyclopropanol 6, was treated with hypochlorite.This observation raised the possibility that 1-aminocyclopropanecarboxylic acids (ACCs) could yield ethylene by a mechanism that involves (1) decarboxylation to a 1-aminocyclopropanol, followed by (2) a fragmentation of the carbinolamine to ethylene induced by a hypochlorite equivalent.Although this mechanism could be ruled out only for 1e, no evidence could be found for it in the reactions of other ACCs, 1a-f, with hypochlorite.The fact that 1b-cis-2,3-d2 yieldedonly ethylene-cis-1,2-d2 is consistent with either the mechanism described above or a nitrenium ion mechanism.In the reaction of cyclopropanamines with neutral hypochlorite, ethylene is not the major product.From the primary and secondary amino acids 1a-c, a 3-hydroxypropanenitrile or propanamide, 2a-c, probably the product of a nucleophilic ring-opening step followed by decarboxylation, is formed.Similar products are formed from other cyclopropanamines: 2a from 1g, 2d from 1h, 2e and 2f from 1i, and lactone 5 from 1j.
