135777-18-3 Usage
General Description
N-Dodecanoyl-4-hydroxy-L-proline, also known as dodecanoyl sarcosine, is a chemical compound that belongs to the class of amino acid derivatives. It is commonly used in the cosmetics industry as a surfactant and emulsifying agent due to its ability to reduce the surface tension of liquids and improve the solubility of substances. In addition, it is also utilized in the formulation of various personal care products, such as facial cleansers, shampoos, and skincare creams, to enhance their cleansing and foaming properties. Furthermore, the compound has potential applications in pharmaceuticals as an emulsifier and drug delivery vehicle. Overall, N-Dodecanoyl-4-hydroxy-L-proline is a versatile chemical that serves various functions in the production of consumer products and the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 135777-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,7 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135777-18:
(8*1)+(7*3)+(6*5)+(5*7)+(4*7)+(3*7)+(2*1)+(1*8)=153
153 % 10 = 3
So 135777-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H31NO4/c1-2-3-4-5-6-7-8-9-10-11-16(20)18-13-14(19)12-15(18)17(21)22/h14-15,19H,2-13H2,1H3,(H,21,22)/t14?,15-/m0/s1
135777-18-3Relevant articles and documents
Synthetic studies on L-proline and (4R)-hydroxy-L-proline derivatives
González, Teresa,Abad, Olga,Santano, M. Carmen,Minguillón, Cristina
, p. 1171 - 1182 (2007/10/03)
The preparation of a number of L-proline and (4R)-hydroxy-L-proline derivatives to assess their enantioselectivity when applied to several techniques and experimental conditions is described. All the derivatives prepared incorporated at least one 3,5-disubstituted aromatic ring that contained nitro, chloro or methyl groups and were obtained by classical methods. In spite of the difficulties that arise from the presence of rotational isomers in most cases, the compounds studied are fully described by their 1H and 13C NMR spectra.
