CAS 16202-15-6

(S)-Tropic Acid

CAS : 16202-15-6

Formule : C₉H₁₀O₃

Degré de pureté : 95%

Couleur et forme : Solid

Masse moléculaire : 166.1739

Ref: IN-DA00B5A9

(S)-3-Hydroxy-2-phenylpropanoic acid

CAS : 16202-15-6

(S)-3-Hydroxy-2-phenylpropanoic acid

Degré de pureté : 98%

Masse moléculaire : 166.17g/mol

Ref: 54-OR87242

Atropine Impurity 2 ((-)-S-Tropic Acid)

CAS : 16202-15-6

Formule : C₉H₁₀O₃

Masse moléculaire : 166.18

Ref: 4Z-A-151010

(S)-3-Hydroxy-2-phenylpropanoic acid

CAS : 16202-15-6

Formule : C₉H₁₀O₃

Degré de pureté : 98%

Masse moléculaire : 166.176

Ref: 10-F549441

(S)-Tropic Acid

Produit contrôlé

CAS : 16202-15-6

Formule : C₉H₁₀O₃

Couleur et forme : Neat

Masse moléculaire : 166.174

Ref: TR-T892625

(-)-S-Tropic Acid

CAS : 16202-15-6

Formule : C₉H₁₀O₃

Masse moléculaire : 166.18

Ref: ST-EA-CP-A206025

(2S)-3-Hydroxy-2-phenylpropanoic acid

CAS : 16202-15-6

(2S)-3-Hydroxy-2-phenylpropanoic acid is an unlabelled, naturally occurring compound. It is the citric acid analog of L-phenylalanine. The structure of (2S)-3-Hydroxy-2-phenylpropanoic acid is a skeleton that consists of one hydroxyl group and one carboxylic acid group. The carboxylic acid group has a double bond in the alpha position to the carboxyl carbon, which gives this molecule an acidic character. The chloride ion is also present in this structure. This molecule can be synthesized by a kinetic reaction that involves fatty acids and brugmansia as catalysts. It can also be synthesized through a catalysed reaction using thionyl chloride as a catalyst.

Formule : C₉H₁₀O₃

Degré de pureté : Min. 95%

Masse moléculaire : 166.17 g/mol

Ref: 3D-RAA20215