610299-77-9 Usage
Description
L-Proline, 1-(2-propenyl)(9CI) is a chemical compound with the molecular formula C9H15NO2. It is a derivative of the amino acid proline, with an additional 2-propenyl group attached to the nitrogen atom. L-Proline, 1-(2-propenyl)(9CI) is known for its role in the synthesis of proteins and peptides, and its ability to stabilize the structure of collagen. L-Proline, 1-(2-propenyl)(9CI) is also used in the development of various drugs and dietary supplements, and is considered to have potential therapeutic properties.
Uses
Used in Pharmaceutical Industry:
L-Proline, 1-(2-propenyl)(9CI) is used as an active pharmaceutical ingredient for the development of various drugs. Its potential therapeutic properties make it a valuable compound in the creation of new medications.
Used in Food Additive Industry:
L-Proline, 1-(2-propenyl)(9CI) is used as a food additive to enhance the flavor and texture of certain products. Its ability to stabilize the structure of collagen can also contribute to the improvement of food quality.
Used in Dietary Supplements:
L-Proline, 1-(2-propenyl)(9CI) is used as a dietary supplement to support protein synthesis and collagen production in the body. Its potential health benefits make it a popular ingredient in various nutritional products.
Check Digit Verification of cas no
The CAS Registry Mumber 610299-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,2,9 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 610299-77:
(8*6)+(7*1)+(6*0)+(5*2)+(4*9)+(3*9)+(2*7)+(1*7)=149
149 % 10 = 9
So 610299-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-2-5-9-6-3-4-7(9)8(10)11/h2,7H,1,3-6H2,(H,10,11)/t7-/m0/s1
610299-77-9Relevant articles and documents
Facile removal strategy for allyl and allyloxycarbonyl protecting groups using solid-supported barbituric acid under palladium catalysis
Tsukamoto, Hirokazu,Suzuki, Takamichi,Kondo, Yoshinori
, p. 1105 - 1108 (2007/10/03)
Solid-supported barbituric acid can be used for the palladium(0)-catalyzed deprotection of allyl amines, carbamates, carbonates, esters and ethers. This solid-supported reagent facilitates isolation and purification of the deprotected compounds, especially acids and amines.