CAS 14173-40-1

Phenylalanine, 4-chloro-, methyl ester, hydrochloride (1:1)

Description:

Phenylalanine, 4-chloro-, methyl ester, hydrochloride (1:1) is a chemical compound characterized by its structure, which includes a phenylalanine backbone modified by a chlorine atom at the para position and a methyl ester functional group. This compound is typically encountered as a hydrochloride salt, which enhances its solubility in water and may influence its stability and reactivity. The presence of the chlorine substituent can affect the compound's biological activity and interaction with enzymes or receptors. As an amino acid derivative, it may play a role in various biochemical processes, including protein synthesis and metabolic pathways. The methyl ester form suggests potential applications in medicinal chemistry, where it may serve as a prodrug or a building block for more complex molecules. Safety and handling precautions should be observed, as with many chemical substances, due to potential toxicity or reactivity. Overall, this compound is of interest in both research and pharmaceutical contexts, particularly in studies related to amino acid metabolism and drug design.

Formula: C₁₀H₁₂ClNO₂·ClH

InChI: InChI=1S/C10H12ClNO2.ClH/c1-14-10(13)9(12)6-7-2-4-8(11)5-3-7;/h2-5,9H,6,12H2,1H3;1H

InChI key: InChIKey=GCBCWTWQAFLKJG-UHFFFAOYSA-N

SMILES: C(C(C(OC)=O)N)C1=CC=C(Cl)C=C1.Cl

Synonyms:

• (2R)-3-(4-chlorophenyl)-1-methoxy-1-oxopropan-2-aminium
• (2S)-3-(4-chlorophenyl)-1-methoxy-1-oxopropan-2-aminium
• 3-(4-Chlorophenyl)-1-Methoxy-1-Oxopropan-2-Aminium Chloride
• 4-Chloro-DL-Phe-OMe・HCl
• 4-Chlorophenylalanine methyl ester hydrochloride
• <span class="text-smallcaps">DL</span>-(4-Chlorophenyl)alanine methyl ester hydrochloride
• <span class="text-smallcaps">DL</span>-(p-Chlorophenyl)alanine methyl ester hydrochloride
• <span class="text-smallcaps">DL</span>-Phenylalanine, 4-chloro-, methyl ester, hydrochloride
• Alanine, 3-(p-chlorophenyl)-, methyl ester, hydrochloride, <span class="text-smallcaps">DL</span>-
• Alanine, 3-(p-chlorophenyl)-, methyl ester, hydrochloride, DL-
• DL-3-(p-Chlorophenyl)alanine methyl ester hydrochloride
• DL-4-chlorophenylalanine methyl ester hydrochloride
• DL-Pcpa methyl ester hydrochloride
• DL-Phenylalanine, 4-chloro-, methyl ester, hydrochloride
• DL-p-Chlorophenylalanine methyl ester hydrochloride
• H-DL-Phe(4-Cl)-OMe・HCl
• Methyl 4-Chlorophenylalaninate
• Phenylalanine, 4-chloro-, methyl ester, hydrochloride
• Phenylalanine, 4-chloro-, methyl ester, hydrochloride (1:1)
• p-Chlorophenylalanine methyl ester hydrochloride
• Methyl 4-chloro-3-phenyl-DL-alaninate hydrochloride

Phenylalanine, 4-chloro-, methyl ester, hydrochloride (1:1)

CAS: 14173-40-1

Formula: C₁₀H₁₃Cl₂NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 250.1217

Ref: IN-DA001GY1

Methyl 2-Amino-3-(4-Chlorophenyl)Propanoate Hydrochloride

CAS: 14173-40-1

Methyl 2-Amino-3-(4-Chlorophenyl)Propanoate Hydrochloride

Purity: 98%

Molecular weight: 250.12g/mol

Ref: 54-OR1013786

pCPA methyl ester hydrochloride

CAS: 14173-40-1

pCPA methyl ester hydrochloride

Purity: ≥98%

Molecular weight: 250.12g/mol

Ref: 54-BUP17885

4-Chloro-DL-Phe-Ome hydrochloride

CAS: 14173-40-1

Formula: ClC₆H₄CH₂CH(NH₂)CO₂CH₃·HCl

Molecular weight: 250.12

Ref: 7W-GM7869

pCPA methyl ester hydrochloride

CAS: 14173-40-1

pCPA methyl ester HCl inhibits tryptophan hydroxylase, 5-HT synthesis, crosses blood-brain barrier, lowers central 5-HT.

Formula: C₁₀H₁₃Cl₂NO₂

Purity: 99.73% - 99.88%

Color and Shape: Solid

Molecular weight: 250.12

Ref: TM-T41143

4-Chloro-DL-phenylalanine methyl ester hydrochloride

CAS: 14173-40-1

4-Chloro-DL-phenylalanine methyl ester hydrochloride is a dopamine receptor agonist that has been shown to have antinociceptive properties in animal models of pain. It has also been shown to inhibit the release of lactogenic hormones, which are hormones that stimulate milk production. Dopamine is a neurotransmitter that plays a role in locomotor activity and reward mechanisms. 4-Chloro-DL-phenylalanine methyl ester hydrochloride binds to the dopamine receptor, inducing activation of the G protein and subsequent phospholipase C activation. This stimulates the synthesis of inositol triphosphate (IP3) and diacylglycerol (DAG). IP3 causes an increase in intracellular calcium ions, leading to muscle contraction, while DAG activates protein kinase C (PKC), which can inhibit adenyl cyclase and thus lead to decreased cAMP levels. The 5HT2A

Formula: C₁₀H₁₂ClNO₂·HCl

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 250.10 g/mol

Ref: 3D-FC47677

4-Chloro-DL-Phe-OMe.HCl

CAS: 14173-40-1

M03172 - 4-Chloro-DL-Phe-OMe.HCl

Formula: C₁₀H₁₃Cl₂NO₂

Purity: 98%

Color and Shape: Solid, White powder

Molecular weight: 250.12

Ref: 10-M03172