61847-07-2 Usage
Uses
Used in Pharmaceutical Industry:
(S)-4-BROMO-1,2-EPOXYBUTANE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of complex organic molecules that can be utilized in the development of new drugs and medications.
Used in Organic Synthesis:
In the field of organic chemistry, (S)-4-BROMO-1,2-EPOXYBUTANE is used as a reagent in organic synthesis reactions. Its epoxide functional group can undergo ring-opening reactions with various nucleophiles, enabling the formation of new chemical bonds and the synthesis of a wide range of organic compounds.
Used in Laboratory Research:
(S)-4-BROMO-1,2-EPOXYBUTANE is employed in laboratory research as a reagent for conducting various organic synthesis reactions. Its versatility in forming new chemical bonds makes it a valuable tool for chemists in exploring new reaction pathways and developing novel organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 61847-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,4 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61847-07:
(7*6)+(6*1)+(5*8)+(4*4)+(3*7)+(2*0)+(1*7)=132
132 % 10 = 2
So 61847-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H7BrO/c5-2-1-4-3-6-4/h4H,1-3H2/t4-/m0/s1
61847-07-2Relevant academic research and scientific papers
Synthesis of a variety of optically active hydroxylated heterocyclic compounds using epoxide hydrolase technology
Pienaar, Daniel P.,Mitra, Robin K.,Deventer, Thomas I. van,Botes, Adriana L.
body text, p. 6752 - 6755 (2009/04/06)
Novel epoxide hydrolases in Yarrowia lipolytica have been shown to hydrolyse a variety of functionalised epoxides with good to excellent stereoselectivity and at high volumetric productivities. Individual biotransformation products have been converted into optically active (R)-(tetrahydrofuran-2-yl)methanol (6), (S)-N-benzyl-3-hydroxypyrrolidine (7), (S)-3-hydroxytetrahydrothiophene (8), (S)-N-benzyl-3-acetoxypiperidine (10), (S)-3-hydroxytetrahydrofuran (16) and (R)-[(S)-N-benzylpyrrolidin-2-yl](phenyl)methanol (20).
