233608-12-3 Usage
Description
(R)-1-(4-bromophenyl)prop-2-en-1-amine hydrochloride is a chiral chemical compound featuring a propenylamine group with a 4-bromophenyl substituent and a hydrochloride salt. As the (R)-enantiomer, it holds the active form and is known for its potential applications in organic synthesis and pharmaceutical research. (R)-1-(4-bromophenyl)prop-2-en-1-amine hydrochloride can serve as a building block for synthesizing various compounds with pharmacological activity, and its hydrochloride salt form enhances its solubility in water, which may be beneficial for specific applications.
Uses
Used in Organic Synthesis:
(R)-1-(4-bromophenyl)prop-2-en-1-amine hydrochloride is used as a building block in organic synthesis for the creation of various compounds with pharmacological activity. Its unique structure and reactivity make it a valuable component in the development of new molecules with potential therapeutic uses.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (R)-1-(4-bromophenyl)prop-2-en-1-amine hydrochloride is used as a key intermediate in the development of new drugs. Its chiral nature and the presence of the bromophenyl group provide opportunities for the design and synthesis of novel therapeutic agents, particularly those targeting specific receptors or enzymes in the body.
Used in Drug Delivery Systems:
(R)-1-(4-bromophenyl)prop-2-en-1-amine hydrochloride's enhanced solubility due to its hydrochloride salt form can be utilized in drug delivery systems to improve the bioavailability and efficacy of the synthesized compounds. This property may be particularly useful in the development of targeted drug delivery systems, where the compound's solubility can facilitate better absorption and distribution within the body.
Check Digit Verification of cas no
The CAS Registry Mumber 233608-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,6,0 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 233608-12:
(8*2)+(7*3)+(6*3)+(5*6)+(4*0)+(3*8)+(2*1)+(1*2)=113
113 % 10 = 3
So 233608-12-3 is a valid CAS Registry Number.
233608-12-3Relevant articles and documents
Enantioselective, iridium-catalyzed monoallylation of ammonia
Pouy, Mark J.,Stanley, Levi M.,Hartwig, John F.
, p. 11312 - 11313 (2011/03/19)
(Chemical Equation Presented) Highly enantioselective, iridium-catalyzed monoallylations of ammonia are reported. These reactions occur with electron-neutral, -rich, and -poor cinnamyl carbonates, alkyl and trityloxy-substituted allylic carbonates, and di
Synthesis of α-arylalkylamines by addition of Grignard reagents to N- (diethoxyphosphoryl)aldimines
Zwierzak, Andrzej,Napieraj, Anna
, p. 930 - 934 (2007/10/03)
Addition of organomagnesium bromides to N-(diethoxyphosphoryl) aldimines 1 carded out in tetrahydrofuran at 20-25°C affords diethyl N-alkyl- phosphoramidates 2a-w in high yields and spectroscopic purity. Deprotection of the latent amino groups in 2 results in the formation of α-arylalkylamine hydrochlorides 3a-w.
