CAS 64318-28-1

N-Boc-tyramine

Description:

N-Boc-tyramine is a chemical compound characterized by its structure, which includes a tyramine backbone modified with a tert-butyloxycarbonyl (Boc) protecting group. This modification enhances its stability and solubility, making it useful in various synthetic applications, particularly in organic chemistry and pharmaceutical research. The Boc group is commonly used to protect amines during chemical reactions, allowing for selective functionalization of other reactive sites. N-Boc-tyramine is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide (DMSO). It is often employed in the synthesis of more complex molecules, including peptides and other bioactive compounds. The compound's reactivity is influenced by the presence of the amino group, which can participate in various reactions, including acylation and coupling reactions. As with many chemical substances, proper handling and safety precautions should be observed, as it may pose health risks if not managed appropriately.

Formula: C₁₃H₁₉NO₃

InChI: InChI=1/C13H19NO3/c1-13(2,3)17-12(16)14-9-8-10-4-6-11(15)7-5-10/h4-7,15H,8-9H2,1-3H3,(H,14,16)

SMILES: CC(C)(C)OC(=NCCc1ccc(cc1)O)O

Synonyms:

• [2-(4-Hydroxyphenyl)ethyl]carbamic acid tert-butyl ester
• Tert-Butyl [2-(4-Hydroxyphenyl)Ethyl]Carbamate
• Boc-Tyramine

N-(tert-Butoxycarbonyl)tyramine

CAS: 64318-28-1

Formula: C₁₃H₁₉NO₃

Purity: >97.0%(GC)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 237.30

Ref: 3B-B3512

tert-Butyl 4-hydroxyphenethylcarbamate

CAS: 64318-28-1

Formula: C₁₃H₁₉NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 237.2949

Ref: IN-DA003SU9

tert-Butyl 4-hydroxyphenethylcarbamate

CAS: 64318-28-1

tert-Butyl 4-hydroxyphenethylcarbamate

Purity: 97%

Molecular weight: 237.30g/mol

Ref: 54-OR75169

N-tert-Butoxycarbonyl tyramine

CAS: 64318-28-1

N-tert-Butoxycarbonyl tyramine is a molecule that has been shown to have anti-tuberculosis properties. It is synthesized by reacting N-Boc-tyrosine with chloroform in the presence of an acid catalyst. The reaction product is a zwitterion, which can be converted to an ionic form by treatment with mineral acids or phosphoric acid. The chloride ion is released from the molecule and reacts with phosphate ions to form hydroxyapatite, which is used as a bone substitute. This compound also has potential for use in cancer treatments due to its ability to inhibit cell proliferation and induce apoptosis in cancer cells. The uptake of this drug was studied using caco-2 cells cultured on plastic membrane inserts in contact with phosphate buffered saline (PBS). The results showed that it had a high uptake rate and concentration in these cells. This compound was also found to have an inhibitory effect on phosphatase

Formula: C₁₃H₁₉NO₃

Purity: Min. 95%

Molecular weight: 237.29 g/mol

Ref: 3D-FB19405

N-tert-Butoxycarbonyl Tyramine

Controlled Product

CAS: 64318-28-1

Formula: C₁₃H₁₉NO₃

Color and Shape: Neat

Molecular weight: 237.29

Ref: TR-B690580

Boc-Tyramine

CAS: 64318-28-1

Formula: C₁₃H₁₉NO₃

Purity: 97%

Color and Shape: Crystalline Powder,Powder

Molecular weight: 237.299

Ref: 10-F048713