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N-succinimidyl-3-(tri-n-butylstannyl)benzoate

Basic Information

  • CAS No.: 112725-22-1
  • Purity: 99%
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1.What is the N-succinimidyl-3-(tri-n-butylstannyl)benzoate ?

Used in Organic Synthesis:
N-succinimidyl-3-(tri-n-butylstannyl)benzoate is used as a crosslinking agent for the introduction of the stannyl moiety into organic molecules, facilitating further functionalization and manipulation.
Used in Chemical Modification of Biomolecules:
N-succinimidyl-3-(tri-n-butylstannyl)benzoate is used as a coupling reagent in bioconjugation reactions, allowing for the attachment of specific functional groups to biomolecules.
Used in Pharmaceutical Industry:
N-succinimidyl-3-(tri-n-butylstannyl)benzoate is used as a reagent for the synthesis of radioimaging agents and pharmaceuticals, enhancing their binding properties and improving their therapeutic outcomes.
Used in Chemical Biology Research:
N-succinimidyl-3-(tri-n-butylstannyl)benzoate is used as a reagent for the modification of proteins and peptides, making it a versatile tool for chemical biology and medicinal chemistry research.

bis(tri-n-butyltin)
813-19-4

bis(tri-n-butyltin)

2,5-dioxopyrrolidin-1-yl 3-iodobenzoate
91487-18-2

2,5-dioxopyrrolidin-1-yl 3-iodobenzoate

N-succinimidyl 3-(tri-n-butyl)stannylbenzoate
112725-22-1

N-succinimidyl 3-(tri-n-butyl)stannylbenzoate

Conditions
Conditions Yield
tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; toluene; for 24h; Inert atmosphere; Reflux;
46%
N-succinimidyl 3-(tri-n-butyl)stannylbenzoate
112725-22-1

N-succinimidyl 3-(tri-n-butyl)stannylbenzoate

1-(2-(5-(2-methoxyethoxy)-1H-benzo[d]imidazol-1-yl)quinolin-8-yl)piperidin-4-amine

1-(2-(5-(2-methoxyethoxy)-1H-benzo[d]imidazol-1-yl)quinolin-8-yl)piperidin-4-amine

N-3-(tributylstannyl)benzoyl-1-{2-[5-(2-methoxyethoxy)-1H-benzo[d]imidazol-1-yl]-quinolin-8-yl}piperidin-4-amine

N-3-(tributylstannyl)benzoyl-1-{2-[5-(2-methoxyethoxy)-1H-benzo[d]imidazol-1-yl]-quinolin-8-yl}piperidin-4-amine

Conditions
Conditions Yield
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 50 ℃; for 3h; Inert atmosphere;
56%

2.What is the CAS number for N-succinimidyl-3-(tri-n-butylstannyl)benzoate ?

The CAS number of N-succinimidyl-3-(tri-n-butylstannyl)benzoate is 112725-22-1.

More information of N-succinimidyl-3-(tri-n-butylstannyl)benzoate 112725-22-1 are:

CAS?Number

112725-22-1

Boiling Point

528°C at 760 mmHg

Flash Point

273.2°C

Vapor Pressure

3.08E-11mmHg at 25°C

PSA

63.68000

LogP

4.59110

3.What are another words for N-succinimidyl-3-(tri-n-butylstannyl)benzoate ?

Synonyms?for?N-succinimidyl-3-(tri-n-butylstannyl)benzoate 112725-22-1:2,5-Pyrrolidinedione,1-[[3-(tributylstannyl)benzoyl]oxy]- (9CI)

4.What is the molecular formula of N-succinimidyl-3-(tri-n-butylstannyl)benzoate?

The chemical formula of ?N-succinimidyl-3-(tri-n-butylstannyl)benzoate is?C23H35 N O4 Sn which containing 23 Carbon atoms,35 Hydrogen atoms,1 Nitrogen atoms,4 Oxygen atoms and 1 Tin atoms,and the molecular weight of??N-succinimidyl-3-(tri-n-butylstannyl)benzoate?is 508.245.

5.What is N-succinimidyl-3-(tri-n-butylstannyl)benzoate (112725-22-1) used for?

N-succinimidyl-3-(tri-n-butylstannyl)benzoate is a chemical compound that is commonly used in organic synthesis and chemical modification of biomolecules. It belongs to the family of succinimidyl esters, which are widely utilized as crosslinking agents and coupling reagents in bioconjugation reactions. The presence of the tri-n-butylstannyl group makes N-succinimidyl-3-(tri-n-butylstannyl)benzoate particularly useful for the introduction of the stannyl moiety into organic molecules, enabling further functionalization and manipulation.

InChI:InChI=1/C11H8NO4.3C4H9.Sn/c13-9-6-7-10(14)12(9)16-11(15)8-4-2-1-3-5-8;3*1-3-4-2;/h1-2,4-5H,6-7H2;3*1,3-4H2,2H3;/rC23H35NO4Sn/c1-4-7-15-29(16-8-5-2,17-9-6-3)20-12-10-11-19(18-20)23(27)28-24-21(25)13-14-22(24)26/h10-12,18H,4-9,13-17H2,1-3H3

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