4151-03-5 Usage
General Description
Methyl 2-methyl-3-(pyrrolidin-1-yl)propanoate is a chemical compound that belongs to the class of esters. It is a colorless liquid with a fruity odor and is commonly used as a fragrance and flavoring agent in various consumer products. It is also used in the synthesis of pharmaceuticals and other fine chemicals. METHYL 2-METHYL-3-(PYRROLIDIN-1-YL)PROPANOATE has potential applications in the food, cosmetic, and pharmaceutical industries as a fragrance ingredient and flavor additive. Additionally, it is used in the production of perfumes, soaps, and other personal care products due to its pleasant aroma.
Check Digit Verification of cas no
The CAS Registry Mumber 4151-03-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4151-03:
(6*4)+(5*1)+(4*5)+(3*1)+(2*0)+(1*3)=55
55 % 10 = 5
So 4151-03-5 is a valid CAS Registry Number.
4151-03-5Relevant articles and documents
SEGREGATED FLUORINATED ESTERS
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Page/Page column 32, (2016/05/24)
Segregated fluorinated esters are described that are useful as dielectric fluids in electrical devices and as heat transfer agents.
Aza-michael addition of amines to α,β-unsaturated compounds using molecular iodine as catalyst
Borah, Kalyan Jyoti,Phukan, Mridula,Borah, Ruli
experimental part, p. 2830 - 2836 (2010/11/02)
Aza-Michael adducts are obtained in very good yields by the conjugate addition of aliphatic amines to α,β-unsaturated compounds using molecular iodine as catalyst in dichloromethane at room temperature. Aromatic amines were found to be reactive under reflux in toluene.
Significant rate acceleration of the aza-Michael reaction in water
Ranu, Brindaban C.,Banerjee, Subhash
, p. 141 - 143 (2007/10/03)
The addition of amines to conjugated alkenes has been carried out in water at room temperature very efficiently without any catalyst. Significant rate acceleration of this reaction is observed in water compared to organic solvents.
