125582-80-1 Usage
General Description
1-Benzylamino-but-3-en-2-ol is a compound with the chemical formula C11H15NO and a molecular weight of 177.24 g/mol. It is a versatile chemical that is commonly used in organic synthesis and pharmaceutical research. It is derived from 3-buten-2-ol and contains a benzylamine group, making it a valuable building block for the production of various pharmaceuticals and biologically active molecules. Its unique structure and reactivity make it a valuable tool in the development of new drugs and therapeutic agents. Additionally, 1-Benzylamino-but-3-en-2-ol has demonstrated potential antibacterial and antifungal properties, making it a promising candidate for further research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 125582-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,8 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125582-80:
(8*1)+(7*2)+(6*5)+(5*5)+(4*8)+(3*2)+(2*8)+(1*0)=131
131 % 10 = 1
So 125582-80-1 is a valid CAS Registry Number.
125582-80-1Relevant articles and documents
A synthetic strategy toward eight-membered cyclic amines by cycloetherification and claisen rearrangement
Han, Seo-Jung,Cavitt, Marchello A.,Stoltz, Brian M.
, p. 3300 - 3303 (2021)
Eight-membered nitrogen-containing heterocycles were straightforwardly produced by a nickel-catalyzed cycloetherification and subsequent Claisen rearrangement of secondary and tertiary alcohols. In particular, a one-pot transformation was achieved with tertiary alcohols in moderate to good yields. This operationally simple reaction is tolerant of many functional groups and applicable to the synthesis of various medium-sized ring nitrogen-containing heterocycles.
AMINOLEAD COMPOUNDS AS A NEW REAGENT FOR REGIOSELECTIVE RING OPENING OF EPOXIDES
Yamada, Jun-ichi,Yumoto, Masatoshi,Yamamoto, Yoshinori
, p. 4255 - 4258 (2007/10/02)
Regioselective ring opening of epoxides is accomplished by using aminolead compounds; the reagents attack the less hindered carbon of epoxide ring, and the amino alcohols are obtained in good yields.