1185294-54-5 Usage
General Description
1-Methoxy-3-Methyl-2-Butanamine Hydrochloride is a chemical compound that is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It is also known for its use as a reagent in various chemical reactions, including the formation of amides and esters. 1-METHOXY-3-METHYL-2-BUTANAMINE HYDROCHLORIDE is a hydrochloride salt, which means it is in a stable and soluble form, making it easier to handle and use in various applications. It is important to handle this compound with care, as it may be harmful if ingested, inhaled, or comes into contact with the skin or eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 1185294-54-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,2,9 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1185294-54:
(9*1)+(8*1)+(7*8)+(6*5)+(5*2)+(4*9)+(3*4)+(2*5)+(1*4)=175
175 % 10 = 5
So 1185294-54-5 is a valid CAS Registry Number.
1185294-54-5Relevant articles and documents
Mild N-deacylation of secondary amides by alkylation with organocerium reagents
Wang, Ai-E.,Chang, Zong,Liu, Yong-Peng,Huang, Pei-Qiang
supporting information, p. 1055 - 1058 (2015/09/01)
Secondary amides are a class of highly stable compounds serving as versatile starting materials, intermediates and directing groups (amido groups) in organic synthesis. The direct deacylation of secondary amides to release amines is an important transformation in organic synthesis. Here, we report a protocol for the deacylation of secondary amides and isolation of amines. The method is based on the activation of amides with Tf2O, followed by addition of organocerium reagents, and acidic work-up. The reaction proceeded under mild conditions and afforded the corresponding amines, isolated as their hydrochloride salts, in good yields. In combination with the C-H activation functionalization methodology, the method is applicable to the functionalization of aniline as well as conversion of carboxylic derivatives to functionalized ketones.