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Catalog Number:
00038
CAS Number:
66270-97-1
Ester phénacylique de l'acide 4-(bromométhyl)phénylacétique
Purity:
≥ 97 % (CCM)
Synonym(s):
Phénacyl 4-(bromométhyl)phénylacétate, Ester de PAM
Documents
$75.00 /1G
Taille
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Product Information

Bloc de construction pour la préparation d'un lieur PAM d'acide aminé. L'ester PAM est orthogonalement stable aux conditions de clivage de la plupart des groupes protecteurs utilisés dans FMOC-SPPS.

Synonyms
Phénacyl 4-(bromométhyl)phénylacétate, Ester de PAM
CAS Number
66270-97-1
Purity
≥ 97 % (CCM)
Molecular Formula
C17H15O3Br
Molecular Weight
347.22
MDL Number
MFCD00009632
Melting Point
85 - 91 ºC
Appearance
Poudre jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Phénacyl 4-(bromométhyl)phénylacétate, Ester de PAM
CAS Number
66270-97-1
Purity
≥ 97 % (CCM)
Molecular Formula
C17H15O3Br
Molecular Weight
347.22
MDL Number
MFCD00009632
Melting Point
85 - 91 ºC
Appearance
Poudre jaune clair
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(Bromomethyl)phenylacetic acid phenacyl ester is widely utilized in research focused on:

  • Synthesis of Pharmaceutical Compounds: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs.
  • Drug Delivery Systems: Its unique structure allows for the formulation of drug delivery systems that enhance the bioavailability of therapeutic agents, making treatments more effective.
  • Biochemical Research: Researchers use this compound in biochemical assays to study enzyme interactions and metabolic pathways, providing insights into cellular processes.
  • Material Science: It is employed in the development of advanced materials, including polymers and coatings, that require specific chemical properties for enhanced performance.
  • Organic Synthesis: This chemical is a valuable reagent in organic synthesis, facilitating the creation of complex organic molecules with precision and efficiency.

Citations