17875-18-2 Usage
Description
1-AMINO-3-BUTENE HYDROCHLORIDE, also known as 3-Butenylamine hydrochloride, is an organic compound with the chemical formula C4H10ClN. It is a derivative of 3-butenylamine, where the amine group is protonated and forms a hydrochloride salt. 1-AMINO-3-BUTENE HYDROCHLORIDE is a key intermediate in the synthesis of various organic compounds and pharmaceuticals due to its reactive amine group.
Uses
Used in Pharmaceutical Industry:
1-AMINO-3-BUTENE HYDROCHLORIDE is used as a synthetic intermediate for the production of various pharmaceuticals and active ingredients. Its reactivity allows for the formation of a wide range of amide, imine, and other nitrogen-containing compounds, which are essential in the development of new drugs.
Used in Organic Synthesis:
1-AMINO-3-BUTENE HYDROCHLORIDE is used as a building block in organic synthesis for the preparation of various organic compounds. Its amine group can be alkylated, acylated, or used in other reactions to form a diverse array of molecules with potential applications in various industries.
Used in Chemical Research:
1-AMINO-3-BUTENE HYDROCHLORIDE is used as a research chemical in academic and industrial laboratories. It serves as a model compound for studying the reactivity and properties of amines and their derivatives, as well as a starting material for the development of new synthetic methods and techniques.
Specific Application:
1-AMINO-3-BUTENE HYDROCHLORIDE is used as a reactant in the synthesis of 2-(3-butenylamino)-3-chloronaphthalene-1,4-dione. This is achieved through a reaction with 2,3-dichloro-1,4-naphthoquinone in the presence of sodium bicarbonate, which serves as a base to facilitate the reaction. The resulting compound, 2-(3-butenylamino)-3-chloronaphthalene-1,4-dione, may have potential applications in various fields, such as pharmaceuticals or materials science, depending on its properties and characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 17875-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,7 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17875-18:
(7*1)+(6*7)+(5*8)+(4*7)+(3*5)+(2*1)+(1*8)=142
142 % 10 = 2
So 17875-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N.ClH/c1-2-3-4-5;/h2H,1,3-5H2;1H
17875-18-2Relevant articles and documents
Dimethylamine adducts of allylic triorganoboranes as effective reagents for Petasis-type homoallylation of primary amines with formaldehyde
Kuznetsov, Nikolai Yu.,Tikhov, Rabdan M.,Strelkova, Tatiana V.,Bubnov, Yuri N.
supporting information, p. 7115 - 7119 (2018/10/23)
Dimethylamine adducts of triallyl-, triprenyl- and trans-cinnamyl(dipropyl)borane are effective reagents for mild homoallylation of primary amines with aqueous formaldehyde in MeOH without an inert atmosphere. A new concept is proposed for the explanation of the high stability of allylborane-amine adducts in aqueous MeOH.
Chiral 1,2-dialkenyl diaziridines: Synthesis, enantioselective separation, and nitrogen inversion barriers
Zawatzky, Kerstin,Kamuf, Matthias,Trapp, Oliver
, p. 156 - 162 (2015/03/04)
Trans-1,2-Disubstituted diaziridines form stable enantiomers at ambient conditions because of the two stereogenic pyramidal nitrogen atoms. Functionalized trans-1,2-disubstituted diaziridines can be utilized as a chiral switching moiety between two enantiomeric states in more complex molecular structures. However, the synthesis of functionalized diaziridines is quite challenging, because of the limited tolerance of reaction conditions that can be applied. Here we present a strategy to make trans-1,2-disubstituted diaziridines accessible as versatile building blocks in C-C-bond formations, i.e., the Heck reaction, and therefore introducing aryl substituents. The synthesis of trans-1,2-dialkenyl diaziridines with terminal alkenyl substituents and their stereodynamic properties are described.
Synthesis of 3-oxoazacyclohept-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K
Taillier, Catherine,Hameury, Thomas,Bellosta, Veronique,Cossy, Janine
, p. 549 - 554 (2007/10/03)
The ring-closing metathesis allows the formation of 3-oxoazacyclohept-4-enes from but-3-enamine. By using this methodology, the synthesis of an inhibitor of cathepsin K was achieved in 10 steps from but-3-enamine.
