94339-93-2 Usage
Usage
Coupling agent in the synthesis of various organic molecules
Industries
Pharmaceutical and agrochemical
Function
Facilitating reactions between different functional groups
Configuration
(S)configuration indicating a specific spatial arrangement of atoms
Impact
Affects reactivity and biological properties
Role
Crucial in the production of a wide range of chemical products
Value
Utility in organic synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 94339-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,3 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94339-93:
(7*9)+(6*4)+(5*3)+(4*3)+(3*9)+(2*9)+(1*3)=162
162 % 10 = 2
So 94339-93-2 is a valid CAS Registry Number.
94339-93-2Relevant academic research and scientific papers
SYNTHESIS OF THE OPTICALLY ACTIVE FORMS OF 4,10-DIHYDROXY-1,7-DIOXASPIROUNDECANE AND THEIR CONVERSION TO THE ENANTIOMERS OF 1,7-DIOXASPIROUNDECANE, THE OLIVE FLY PHEROMONE
Mori, Kenji,Uematsu, Tamon,Yanagi, Kazunori,Minobe, Masao
, p. 2751 - 2758 (2007/10/02)
Both the enantiomers of 1,7-dioxaspiroundecane, the major component of the pheromone of the olive fly (Dacus oleae), were synthesized from (S)-malic acid.
SYNTHESIS OF THE ENANTIOMERS OF 1,7-DIOXASPIROUNDECANE AND 4-HYDROXY 1,7-DIOXASPIROUNDECANE, THE COMPONENTS OF THE OLIVE FLY PHEROMONE
Mori, Kenji,Uematsu, Tamon,Watanabe, Hidenori,Yanagi, Kazunori,Minobe, Masao
, p. 3875 - 3878 (2007/10/02)
The enantiomers of the olive fly pheromone (1 and 4) were synthesized from (S)-malic acid in amounts sufficient for the biological test.
