88987-42-2

Basic information

• Product Name: 5-BROMOPENTANOIC ACID, T-BUTYL ESTER
• Synonyms: 5-BROMOPENTANOIC ACID, T-BUTYL ESTER;tert-butyl 5-bromopentanoate;tert-Butyl 5-bromovalerate
• CAS NO: 88987-42-2
• Molecular Formula: C₉H₁₇BrO₂
• Molecular Weight: 237.13408
• Mol File: 88987-42-2.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 93 °C(Press: 1.6 Torr)
• Appearance: /
• Density: 1.223±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 5-BROMOPENTANOIC ACID, T-BUTYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMOPENTANOIC ACID, T-BUTYL ESTER(88987-42-2)
• EPA Substance Registry System: 5-BROMOPENTANOIC ACID, T-BUTYL ESTER(88987-42-2)

Safety Data

• Hazardous Substances Data: 88987-42-2(Hazardous Substances Data)

Usage

Uses

tert-Butyl 5-Bromovalerate is a reactant used in synthetic preparation of haptens for production of monoclonal antibodies for pyraclostrobin ELISA.

Upstream product

• 2067-33-6 5-bromopentanoic acid 
• 115-11-7 isobutene 
• 75-65-0 tert-butyl alcohol 
• 71432-55-8 2-tert-butyl-1,3-diisopropylisourea 
• 4509-90-4 5-bromovaleroyl chloride 

Downstream Products

• 162954-77-0 7-tert-butyl 1-ethyl 2-pimelate 
• 208941-36-0 4-(4-tert-Butoxycarbonyl-butoxy)-benzoic acid benzyl ester 
• 851664-19-2 5-{(S)-3-(4-Chloro-phenyl)-4-[(R)-1-(4-chloro-phenyl)-ethyl]-2,5-dioxo-7-phenyl-2,3,4,5-tetrahydro-[1,4]diazepin-1-yl}-pentanoic acid tert-butyl ester 
• 851664-20-5 5-{(S)-7-(2-Bromo-phenyl)-3-(4-chloro-phenyl)-4-[(R)-1-(4-chloro-phenyl)-ethyl]-2,5-dioxo-2,3,4,5-tetrahydro-[1,4]diazepin-1-yl}-pentanoic acid tert-butyl ester 
• 84451-93-4 8,8-dimethyl-7-oxo-pelargonic acid 
• 212260-29-2 4-(4-Carboxy-butoxy)-benzoic acid 2-(4-hydroxy-3-iodo-phenyl)-ethyl ester 
• 212260-31-6 4-(4-tert-Butoxycarbonyl-butoxy)-benzoic acid 2-(4-hydroxy-3-iodo-phenyl)-ethyl ester 
• 208941-37-1 4-(4-tert-Butoxycarbonyl-butoxy)-benzoic acid 
• 35005-21-1 4-(4-Carboxy-butoxy)-benzoic acid 
• 208941-39-3 4-(4-Carboxy-butoxy)-benzoic acid 3-iodo-benzyl ester 
• 187395-93-3 C₄₉H₆₂N₆O₉S₃ 
• 824957-21-3 5-{3-[(2S*,3S*,5R*)-2-((S)-2-tert-butoxycarbonylaminopropionylamino)-5-butylcarbamoyl-3-hydroxyhexyl]phenoxy}pentanoic acid tert-butyl ester 

Relevant articles and documents

Platinum(II) Complexes of Functionalized Malonato Ligands: Unequivocal Synthesis, Interaction with a Tetradeoxyribonucleotide and Deoxyribonucleic Acid

The unequivocal syntheses of four cis-> complexes has been achieved, avoiding any interaction between the pendant carboxyl group and the platinum.The complexes have been characterized by elemental analysis, 13C NMR and FAB mass spectroscopy.Their interaction with a tetradeoxyribonucleotide d(T-G-G-T) (G = guanosine, T = ribosylthymine) and DNA (in vitro) has been investigated to show that they form adducts of the type 7,N7'>> as do the known therapeutically activeplatinum complexes.However, the presence of the free carbonyl function increases significantly the reactivity with respect to that of the non-functionalized malonato complexes >.

Discovery of ERD-308 as a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Estrogen Receptor (ER)

The estrogen receptor (ER) is a validated target for the treatment of estrogen receptor-positive (ER+) breast cancer. Here, we describe the design, synthesis, and extensive structure-activity relationship (SAR) studies of small-molecule ERα degraders base

Tri-Orthogonal Scaffolds for the Solid-Phase Synthesis of Peptides

Multi-orthogonal scaffolds can be useful for the attachment of several different compounds to the same central skeleton. Such compounds can find applications in the development of protein mimics because of their potential to mimic several distant epitopes