CAS 149490-61-9

N-(Butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-L-tyrosine

Description:

N-(Butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-L-tyrosine, with the CAS number 149490-61-9, is a synthetic compound that belongs to the class of amino acid derivatives. This substance features a tyrosine backbone, which is an aromatic amino acid known for its role in protein synthesis and as a precursor for neurotransmitters. The presence of a butylsulfonyl group suggests that it has sulfonyl functional characteristics, which can enhance solubility and reactivity. Additionally, the incorporation of a pyridine moiety indicates potential interactions with biological targets, possibly influencing its pharmacological properties. The compound may exhibit unique properties such as increased lipophilicity due to the butyl chain, which can affect its bioavailability and distribution in biological systems. Overall, this compound's structural features suggest potential applications in medicinal chemistry, particularly in the development of therapeutic agents targeting specific biological pathways. However, detailed studies would be necessary to fully elucidate its properties and potential uses.

Formula: C₂₂H₃₀N₂O₅S

InChI: InChI=1S/C22H30N2O5S/c1-2-3-16-30(27,28)24-21(22(25)26)17-19-7-9-20(10-8-19)29-15-5-4-6-18-11-13-23-14-12-18/h7-14,21,24H,2-6,15-17H2,1H3,(H,25,26)/t21-/m0/s1

InChI key: InChIKey=FRFFSBHFSQTHRE-NRFANRHFSA-N

SMILES: C([C@H](NS(CCCC)(=O)=O)C(O)=O)C1=CC=C(OCCCCC=2C=CN=CC2)C=C1

Synonyms:

• <span class="text-smallcaps">L</span>-Tyrosine, N-(butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-
• N-(Butylsulfonyl)-O-(4-(4-Piperidinyl)Butyl)-L-Tyrosine
• N-(Butylsulfonyl)-O-[4-(4-Piperidynyl)Butyl]-L-Tyrosine
• N-(Butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-<span class="text-smallcaps">L</span>-tyrosine
• N-(Butylsulfonyl)-O-[4-Pyridin-4-Yl]Butyl]-L-Tyrosine
• L-Tyrosine, N-(butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-
• N-(butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-L-tyrosine
• N-(Butylsulfonyl)-O-[4-(4-pyridinyl)butyl]-L-tyrosine

(S)-2-(Butylsulfonamido)-3-(4-(4-(pyridin-4-yl)butoxy)phenyl)propanoic acid

CAS: 149490-61-9

(S)-2-(Butylsulfonamido)-3-(4-(4-(pyridin-4-yl)butoxy)phenyl)propanoic acid

Formula: C₂₂H₃₀N₂O₅S

Purity: 98%

Molecular weight: 434.55

Ref: 54-OR1123907

(S)-2-(Butylsulfonamido)-3-(4-(4-(pyridin-4-yl)butoxy)phenyl)propanoic acid

CAS: 149490-61-9

Formula: C₂₂H₃₀N₂O₅S

Purity: 99%

Color and Shape: Solid

Molecular weight: 434.5490

Ref: IN-DA001LRH

Tirofiban Impurity 81

CAS: 149490-61-9

Formula: C₂₂H₃₀N₂O₅S

Color and Shape: Yellow Solid

Molecular weight: 434.55

Ref: 4Z-T-1413

N-(n-Butanesulfonyl)-O-[4-(4-pyridinyl)-butyl]-(S)-tyrosine

CAS: 149490-61-9

Applications Tirofiban intermediate.

Formula: C₂₂H₃₀N₂O₅S

Color and Shape: Neat

Molecular weight: 434.55

Ref: TR-B690160

N-(butylsulfonyl)-Tyr(4-(4-pyridinyl)butyl)-OH

CAS: 149490-61-9

(S)-2-(Butylsulfonamido)-3-(4-(4-(pyridin-4-yl)butoxy)phenyl)propanoic acid

Formula: C₂₂H₃₀N₂O₅S

Purity: 98%

Molecular weight: 434.55

Ref: IN-DG9194

N-Butanesulfonyl-O-[4-(4-pyridinyl)-butyl]-(S)-tyrosine

CAS: 149490-61-9

N-Butanesulfonyl-O-[4-(4-pyridinyl)-butyl]-(S)-tyrosine is a synthetic amino acid. It is soluble in water and forms hydrates. The yield of this reaction is 60%. The molecular weight of this compound is 233.3 g/mol. This compound has been shown to have proteolytic activity, which may be due to its ability to cleave peptide bonds in proteins. N-Butanesulfonyl-O-[4-(4-pyridinyl)-butyl]-(S)-tyrosine may also be used as an intermediate for the synthesis of other compounds, such as aminoglycosides and antibiotics. This chemical can be synthesized by reacting L-tyrosine with butanesulfonyl chloride in the presence of sodium hydroxide and an organic base, such as pyridine. The solvents used in this process are chloroform, dich

Formula: C₂₂H₃₀N₂O₅S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 434.55 g/mol

Ref: 3D-FB19373

N-(n-Butanesulfonyl)-O-[4-(4-pyridinyl)-butyl]-(S)-tyrosine

CAS: 149490-61-9

Formula: C₂₂H₃₀N₂O₅S

Molecular weight: 434.55

Ref: ST-EA-CP-T63004