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tert-Butyl 1-(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate CAS:954239-58-8
tert-Butyl 1-(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate is a chemical compound with the molecular formula C16H23NO3. This colorless to pale yellow liquid serves as a valuable building block in organic synthesis due to its unique structure and reactivity. Known for its versatility, this compound finds applications in pharmaceuticals, agrochemicals, and material sciences industries. It is commonly used as an intermediate in the production of complex organic molecules.
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tert-Butyl 3,3,3-trifluoro-2-hydroxypropylcarbamate CAS:1219606-48-0
tert-Butyl 3,3,3-trifluoro-2-hydroxypropylcarbamate is a molecule containing a carbamate linkage connected to a trifluoromethylated alcohol moiety. The electron-withdrawing tert-butyl, trifluoromethyl and hydroxyl substituents impart unique reactivity to this compound. This enables participation in diverse functional group transformations and substitutions reactions.
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1-(3-bromophenyl)-3,3-dimethoxycyclobutane-1-carboxylic acid CAS:2135331-42-7
1-(3-bromophenyl)-3,3-dimethoxycyclobutane-1-carboxylic acid contains a cyclobutane ring fused to a bromophenyl moiety and substituted with two methoxy groups and a carboxylic acid. This complex structure engages in diverse cyclization, substitution, addition, and acid derivative reactions through its multiple reactive sites.
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1-(4-(tert-butoxycarbonyl)phenyl)-3,3-dimethoxycyclobutanecarboxylic acid CAS:
1-(4-(tert-butoxycarbonyl)phenyl)-3,3-dimethoxycyclobutanecarboxylic acid is a cyclobutane derivative containing a carboxylic acid, two methoxy groups and a tert-butoxycarbonyl (Boc) protected phenyl ring. This complex structure allows participation in various substitution, coupling and decarbonylation reactions through its functional handles.
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![[3-(4-Fluoro-phenyl)-isoxazol-5-yl]-Methanol CAS:206055-89-2](https://cdn.globalso.com/xindaobiotech/1ZNB2ZF342ZWRNG244.png)
[3-(4-Fluoro-phenyl)-isoxazol-5-yl]-Methanol CAS:206055-89-2
[3-(4-Fluoro-phenyl)-isoxazol-5-yl]-methanol is an organic compound containing an isoxazole ring linked to a fluorophenyl group and terminating in a hydroxymethyl substituent. This unique structure allows it to engage in a variety of nucleophilic substitution, oxidation, and condensation reactions. The presence of the electron-withdrawing fluorine and reactive alcohol functional group promotes versatile chemistry on this molecule.
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![{[6-(2-methylpyrrolidin-1-yl)pyridin-3-yl]methyl}(propan-2-yl)amine CAS:1270911-03-9](https://cdn.globalso.com/xindaobiotech/1ZNB2ZF342ZWRNG243.png)
{[6-(2-methylpyrrolidin-1-yl)pyridin-3-yl]methyl}(propan-2-yl)amine CAS:1270911-03-9
{[6-(2-Methylpyrrolidin-1-yl)pyridin-3-yl]methyl}(propan-2-yl)amine is a complex organic compound consisting of a pyridine ring substituted with a pyrrolidine and propan-2-ylamine. This elaborate structure allows participation in various substitution, addition and condensation reactions on multiple reacting sites. The pyrrolidine nitrogen and amine moieties especially offer valuable synthetic handles.
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(4-Amino-3-bromophenyl)methanol CAS:146019-46-7
(4-Amino-3-bromophenyl)methanol is a chemical compound used in pharmaceutical, agrochemical, and material science industries. With the molecular formula C7H8BrNO, it appears as a white to off-white solid. Also known as 3-(4-aminophenyl)propan-1-ol, this compound serves as a valuable building block in organic synthesis due to its unique structure and reactivity. Its versatility makes it an essential intermediate for the development of various drugs, agrochemicals, and advanced materials.
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(R)-2-Bromo-1-(4-fluorophenyl)ethanol CAS:1097211-38-5
(R)-2-Bromo-1-(4-fluorophenyl)ethanol is a chiral building block containing a 2-bromoethyl alcohol moiety bonded to a 4-fluorophenyl ring. The presence of the reactive alcohol and bromine groups, along with stereochemical complexity from the R-chirality center, allows this molecule to engage in diverse substitution, addition and resolution reactions.
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(3-(3-Fluorophenyl)isoxazol-5-yl)methanol CAS:954240-02-9
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2-(Ethoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid CAS:132589-66-3
2-(Ethoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid is a organic compound containing an isoquinoline ring system along with a carboxylic acid and ethyl ester functional group. The presence of these reactive groups makes it amenable to a wide range of chemical transformations. The ethyl ester and acid moieties can participate in ester hydrolysis, aminolysis, and acid-base reactions. Additionally, the isoquinoline nucleus provides opportunities for functionalization under various substitution and addition reactions.
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(3-Amino-pyridin-4-yl)-methanol CAS:152398-05-5
The (3-Amino-pyridin-4-yl)-methanol is a versatile chemical compound used in various industries such as pharmaceuticals, agrochemicals, and material sciences. Also known as 3-amino-4-pyridinemethanol, it is a white to off-white solid with the molecular formula C6H8N2O. This compound is widely used as a building block in the synthesis of complex organic molecules due to its unique structure and reactivity. It serves as a key intermediate in the production of pharmaceuticals, especially in the development of novel drugs targeting specific biological pathways.
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(2R,4R)-tert-butyl 4-hydroxy-2-(iodomethyl)pyrrolidine-1-carboxylate CAS:132589-66-3
(2R,4R)-tert-Butyl 4-hydroxy-2-(iodomethyl)pyrrolidine-1-carboxylate is a chiral compound containing a pyrrolidine ring with an alcohol, ester and alkyl halide substituent. The R stereochemistry at the 2 and 4 positions of the ring give it a well-defined three dimensional structure important for biochemical interactions. The alcohol, ester and iodomethyl groups provide multiple reactive sites for organic transformations.
