38042-74-9 Usage
Uses
1-Benzyl-3-Bromopyrrolidine is used as a chemical intermediate in the synthesis of various organic compounds due to its unique structure and functional groups. Its applications can be found in different industries, including pharmaceuticals, agrochemicals, and materials science, where it serves as a building block for the development of new molecules with specific properties and functions.
Used in Pharmaceutical Industry:
1-Benzyl-3-Bromopyrrolidine is used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting specific biological pathways or receptors. Its unique structure and functional groups allow for the creation of novel molecules with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Benzyl-3-Bromopyrrolidine is used as a precursor in the synthesis of active ingredients for pesticides, herbicides, and other crop protection products. Its versatility in chemical reactions enables the development of new molecules with improved efficacy and selectivity.
Used in Materials Science:
1-Benzyl-3-Bromopyrrolidine is utilized in the development of advanced materials with specific properties, such as polymers, coatings, and adhesives. Its unique structure and functional groups contribute to the creation of materials with enhanced performance characteristics, such as improved durability, adhesion, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 38042-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,4 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38042-74:
(7*3)+(6*8)+(5*0)+(4*4)+(3*2)+(2*7)+(1*4)=109
109 % 10 = 9
So 38042-74-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14BrN/c12-11-6-7-13(9-11)8-10-4-2-1-3-5-10/h1-5,11H,6-9H2
38042-74-9Relevant academic research and scientific papers
Stereocontrolled synthesis of 1,2-dialkyl-4-halopyrrolidines through PhSeX-induced cyclization of secondary homoallylamines
Outurquin, Francis,Pannecoucke, Xavier,Berthe, Benedicte,Paulmier, Claude
, p. 1007 - 1014 (2007/10/03)
The selenium-induced cyclization of α-alkyl or α,α-dialkylhomoallyl-benzylamines 1 by use of PhSeX (X = Cl, Br, I; 1.5 equiv.) provided a mixture of (phenylselanylmethyl)azetidines 2 and (phenylselanyl)pyrrolidines 3.[1] When an excess of PhSeX (X = Cl, Br) was used, 4-halopyrrolidines 4 (X = Cl) or 5 (X = Br) were formed and isolated in very good yields. Mono- or dialkyl 4-halopyrrolidines 4 and 5 could also be obtained stereospecifically by SO2Cl2 or Br2 treatment of 4-(phenylselanylmethyl)azetidines 2, by way of the intermediate (halomethyl)azetidines 14 (X = Cl) or 15 (X = Br). When starting from 4-(phenylselanyl)pyrrolidines 3, monoalkylated 4-halopyrrolidines 4 or 5 could be obtained stereospecifically after decomposition of the unstable dihaloselenuranes 16 and 17. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
Synthesis of Functionalized Pyrrolidines from N-(Benzylidene)- and N-(Alkylidene)-homoallylamines
Smaele Dirk De,Kimpe, Norbert De
, p. 2029 - 2030 (2007/10/02)
N-(Benzylidene)- and N-(alkylidene)-homoallylamines are cyclised by electrophiles, e.g. bromine or phenylselenenyl bromide, and by subsequent reduction to the corresponding 3-functionalised pyrrolidines; the stereochemistry was investigated, and reductive
