CAS 81189-61-9

Boc-D-Tyr(2-bromo-Z)-OH

Description:

Boc-D-Tyr(2-bromo-Z)-OH, with the CAS number 81189-61-9, is a chemical compound that features a protected form of the amino acid tyrosine. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, which is commonly used in peptide synthesis to prevent unwanted reactions. The presence of the 2-bromo substituent indicates that this compound has been modified to include a bromine atom at the ortho position of the aromatic ring, which can influence its reactivity and biological activity. The "Z" designation refers to a specific configuration of the double bond in the side chain, indicating a Z (cis) configuration. This compound is typically utilized in organic synthesis and peptide chemistry, particularly in the development of pharmaceuticals and biologically active compounds. Its characteristics include moderate solubility in organic solvents, stability under standard laboratory conditions, and potential reactivity due to the presence of the bromine atom, which can participate in further chemical transformations.

Formula: C₂₂H₂₄BrNO₇

Synonyms:

• Boc-D-Tyr(2-Br-Z)-OH
• N-Tert-Butyloxycarbonyl-O-(2-Bromobenzyloxycarbonyl)-D-Tyrosine

D-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-, (2-bromophenyl)methylcarbonate (ester)

CAS: 81189-61-9

Formula: C₂₂H₂₄BrNO₇

Purity: 95%

Color and Shape: Solid

Molecular weight: 494.3325

Ref: IN-DA00ID65

Boc-D-Tyr(2-Br-Z)-OH

CAS: 81189-61-9

Boc-D-Tyr(2-Br-Z)-OH

Purity: 98%

Molecular weight: 494.34g/mol

Ref: 54-OR1063196

Boc-D-Tyr(2-Br-Z)-OH

CAS: 81189-61-9

Ref: 7W-GM5834

Boc-D-Tyr(Br-Z)-OH

CAS: 81189-61-9

Boc-D-Tyr(Br-Z)-OH is a sugar alcohol that has been shown to have anti-bacterial activity. It has been shown to inhibit the growth of dental plaque by inhibiting the synthesis of oligosaccharides, which are a major component of this type of biofilm. Boc-D-Tyr(Br-Z)-OH also inhibits transfer reactions in the bacterial cell wall, and is therefore able to prevent the formation of cell walls. This compound also has prebiotic properties, which may be due to its ability to stimulate insulin production. The enzyme responsible for Boc-D-Tyr(Br-Z)-OH synthesis is Tools for Peptide Synthesis (TPS). TPS catalyzes a chemical reaction that uses an acceptor molecule (e.g., ATP) and microbial metabolism as substrates. The product of this enzymatic reaction is fatty acids, which are then used in biosynthesis processes such as fatty acid

Formula: C₂₂H₂₄NO₇Br

Purity: Min. 95%

Molecular weight: 494.33 g/mol

Ref: 3D-BDY-2612

Boc-D-Tyr(2-Br-Z)-OH

CAS: 81189-61-9

M06207 - Boc-D-Tyr(2-Br-Z)-OH

Formula: C₂₂H₂₄BrNO₇

Purity: 95%

Color and Shape: No data available.

Molecular weight: 494.338

Ref: 10-M06207

Boc-D-Tyr(2-Br-Z)-OH

CAS: 81189-61-9

Boc-D-Tyr(2-Br-Z)-OH, with catalog number T66218 and CAS number 81189-61-9, is a valuable organic compound for life sciences research.

Formula: C₂₂H₂₄BrNO₇

Color and Shape: Solid

Molecular weight: 494.338

Ref: TM-T66218