103687-30-5 Usage
Chiral compound
Yes
A chiral compound is one that has a chiral center, which means it cannot be superimposed on its mirror image. This compound has two asymmetric carbon atoms (1R and 2S), making it chiral.
Asymmetric carbon atoms
1R and 2S
These designations indicate the configuration of the chiral centers in the molecule. The R and S notations are based on the Cahn-Ingold-Prelog priority rules, which determine the absolute configuration of a chiral center.
Applications
Pharmaceutical synthesis, specialty chemicals, cosmetics, personal care products, polymer synthesis, flavors, and fragrances
This compound is used as a building block in various industries due to its versatile chemical properties and biological activities.
Biological activities
Antibacterial, antifungal, and antiviral properties
The compound exhibits a range of biological activities, making it useful in the development of pharmaceuticals and other products with these properties.
Potential uses
Wide range of applications in different industries
Due to its unique properties and activities, 1,2-Nonanediol, 1-phenyl-, (1R,2S)-relhas potential applications in various fields, including pharmaceuticals, cosmetics, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 103687-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,8 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103687-30:
(8*1)+(7*0)+(6*3)+(5*6)+(4*8)+(3*7)+(2*3)+(1*0)=115
115 % 10 = 5
So 103687-30-5 is a valid CAS Registry Number.
103687-30-5Relevant articles and documents
Hindered organoboron groups in organic chemistry. 23. The interactions of dimesitylboron stabilised carbanions with aromatic ketones and aldehydes to give alkenes
Pelter,Buss,Colclough,Singaram
, p. 7077 - 7103 (1993)
Dimesitylboron stabilised carbanions react with diarylketones to give the corresponding alkenes in mild conditions with good yields. Reactions with aromatic aldehydes are more complex, but in all cases E-alkenes are available in good yields by trapping the intermediates with chlorotrimethylsilane followed by treatment with aq. HF/CH3CN. Treatment of the same intermediates with trifluoroacetic anhydride gives mainly the Z-alkenes. The design and mechanisms of these important processes are considered.
THE DIMESITYLBORON GROUP IN ORGANIC SYNTHESIS 7. A UNIQUE VARIANT OF THE BORON-WITTIG REACTION WHICH STEREOSELECTIVELY YIELDS 1,2-DIOLS.
Pelter, Andrew,Buss, Dieter,Pitchford, Andrew
, p. 5093 - 5096 (2007/10/02)
Low temperature oxidation of the intermediates in the Wittig reactions of aryl aldehydes with carbanions stabilised with an adjacent dimesitylboron group leads stereoselectively to erythro-1,2-diols.The mechanistic implications for the boron-Wittig reactions are discussed.
