144404-98-8 Usage
Explanation
Different sources of media describe the Explanation of 144404-98-8 differently. You can refer to the following data:
1. The IUPAC name is a systematic method of naming chemical compounds. It provides information about the structure and arrangement of atoms in the molecule.
2. The common name is a more informal and easily recognizable name for the compound, often used in everyday language.
3. The physical state and color of the compound, which in this case is a colorless liquid.
4. The characteristic smell of the compound, which is described as fruity.
5. The various applications of the compound in different industries, highlighting its versatility.
6. A cautionary note that the compound may pose health risks, emphasizing the need for proper handling and safety precautions.
7. The CAS (Chemical Abstracts Service) number is a unique identifier assigned to a specific chemical compound, used for easy reference and search purposes.
8. The stereochemistry describes the spatial arrangement of atoms in the molecule. In this case, it indicates that the compound has a specific configuration at the chiral center (2S) and a cis arrangement of the substituents around the double bond.
Appearance
Colorless liquid
Odor
Fruity
Uses
Flavoring agent in the food industry, fragrance ingredient in cosmetic and personal care products, chemical intermediate in the synthesis of other compounds
Health Hazards
Potential health hazards
Stereochemistry
(2S-cis)-
Check Digit Verification of cas no
The CAS Registry Mumber 144404-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144404-98:
(8*1)+(7*4)+(6*4)+(5*4)+(4*0)+(3*4)+(2*9)+(1*8)=118
118 % 10 = 8
So 144404-98-8 is a valid CAS Registry Number.
144404-98-8Relevant articles and documents
Distinction of Diastereofaces at the α-Position of Chiral Cyclic Acetals
Tanaka, Naoki,Suemune, Hiroshi,Sakai, Kiyoshi
, p. 1075 - 1086 (2007/10/02)
Key words: chiral acetal; asymmetric 1,2-addition; asymmetric 1,4-addition; C2 symmetry; determination of optical purity; chiral carboxylic acid Asymmetric 1,2- and 1,4-additions to substrates with an acetal as a chiral auxiliary have been studied.Among the tested substrates, C2-symmetrical 5c was most effective for 1,2-addition with MeTi(O-iPr)3.Furthermore, C2-symmetrical carbinol 5b has been found to be a potent 1H-NMR reagent for determination of optical purity of carboxylic acids with a chiral center at the α-position.
