155185-01-6 Usage
Uses
Used in Pharmaceutical Industry:
(R)-1-Azido-4-(Methylsulfinyl)-butane is used as an intermediate in the synthesis of (R)-Sulforaphane (S699105), a compound with potential pharmaceutical applications. Its role in the preparation of (R)-1-Azido-4-(Methylsulfinyl)-butane is crucial for the development of new drugs and therapies.
Used in Chemical Synthesis:
As a chiral building block, (R)-1-Azido-4-(Methylsulfinyl)-butane can be employed in various chemical synthesis processes, particularly in the creation of enantiomerically pure compounds. Its unique structure allows for selective reactions that can lead to the development of new molecules with specific biological activities.
Used in Research and Development:
The compound is also valuable in research and development settings, where it can be used to study the effects of stereochemistry on molecular interactions and biological activities. This can contribute to a better understanding of the underlying mechanisms of various biological processes and the design of more effective drugs and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 155185-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,1,8 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155185-01:
(8*1)+(7*5)+(6*5)+(5*1)+(4*8)+(3*5)+(2*0)+(1*1)=126
126 % 10 = 6
So 155185-01-6 is a valid CAS Registry Number.
155185-01-6Relevant academic research and scientific papers
Enantiopure sulforaphane analogues with various substituents at the sulfinyl sulfur: Asymmetric synthesis and biological activities
Khiar, Noureddine,Werner, Sabine,Mallouk, Siham,Lieder, Franziska,Alcudia, Ana,Fernandez, Inmaculada
experimental part, p. 6002 - 6009 (2009/12/26)
(Chemical Equation Presented) A convergent and high-yielding approach for the asymmetric synthesis of sulforaphane 2 and four analogues differently substituted at the sulfinyl sulfur has been developed. The key step of the synthesis is the diastereoselect
Asymmetric Synthesis of Chiral Sulfinate Esters and Sulfoxides. Synthesis of Sulforaphane
Whitesell, James K.,Wong, Man-Shing
, p. 597 - 601 (2007/10/02)
Reaction of the chiral auxiliary trans-2-phenylcyclohexanol (1) with thionyl chloride afforded a nearly equal mixture of two diastereomeric chlorosulfite esters (6).Treatment of this mixture with an equivalent amount of a dialkylzinc reagent (Me, Et, i-Pr) afforded high levels of conversion of both chlorosulfite esters to (mainly) a single diastereomer of the sulfinate ester (7).Levels of absolute stereochemical induction ranged from 10:1 to 96:4 under conditions affording high chemical yields.The method was employed for the separate synthesis of both enantiomers of sulforaphane (13).
