1213693-68-5 | (S)-Cyclopropyl(4-methoxyphenyl)methanamine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	2 weeks	$284.00	$199.00
5mg	95%	2 weeks	$303.00	$212.00
10mg	95%	2 weeks	$338.00	$237.00

Description

• Catalog Number: AE43557
• Chemical Name: (S)-Cyclopropyl(4-methoxyphenyl)methanamine hydrochloride
• CAS Number: 1213693-68-5
• Molecular Formula: C11H16ClNO
• Molecular Weight: 213.7038
• MDL Number: MFCD11101160
• SMILES: COc1ccc(cc1)[C@H](C1CC1)N.Cl

Computed Properties

• Complexity: 160
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

(S)-Cyclopropyl(4-methoxyphenyl)methanamine hydrochloride, also known as $name$, is a valuable compound in chemical synthesis due to its versatile applications. This compound is widely used as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its unique stereochemistry makes it a key intermediate in the production of various biologically active molecules.In chemical synthesis, (S)-Cyclopropyl(4-methoxyphenyl)methanamine hydrochloride serves as a crucial starting material for the preparation of enantiomerically pure compounds. Its cyclopropyl ring provides a compact and rigid structure, which can influence the stereochemistry and reactivity of the resulting products. By incorporating this compound into synthetic routes, chemists can control the stereochemical outcome of reactions, leading to the production of specific enantiomers with enhanced biological activity or selectivity.Furthermore, (S)-Cyclopropyl(4-methoxyphenyl)methanamine hydrochloride can be utilized in the construction of complex molecules through strategic functional group transformations. Its methoxyphenyl group can serve as a handle for further derivatization, allowing for the introduction of additional substituents or functional groups to tailor the properties of the final compound. This versatility makes it a valuable building block for the creation of diverse chemical structures in organic synthesis.Overall, the application of (S)-Cyclopropyl(4-methoxyphenyl)methanamine hydrochloride in chemical synthesis offers chemists a powerful tool for accessing enantiomerically pure compounds and structurally complex molecules with potential pharmaceutical or agrochemical relevance. This compound plays a vital role in advancing the field of synthetic chemistry and facilitating the development of novel bioactive substances.