185456-26-2

Basic information

• Product Name: BOC3-HYDRAZINE
• Synonyms: TRIS-(T-BUTYLOXYCARBONYL)-HYDRAZINE;TRIS-(TERT-BUTYLOXYCARBONYL)-HYDRAZINE;TRIS-BOC-HYDRAZINE;BOC3-HYDRAZINE;tri-tert-Butyl hydrazine-1,1,2-tricarboxylate;Tert-butyl N-[(2-methylpropan-2-yl)oxycarbonyl]-n-[(2-methylpropan-2-yl)oxycarbonylamino]carbamate;1,1,2-Tris(tert-butoxycarbonyl)hydrazine
• CAS NO: 185456-26-2
• Molecular Formula: C₁₅H₂₈N₂O₆
• Molecular Weight: 332.39
• Mol File: 185456-26-2.mol

Chemical Properties

• Melting Point: 109-110 °C
• Appearance: /
• Density: 1.097±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 7.34±0.50(Predicted)
• CAS DataBase Reference: BOC3-HYDRAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: BOC3-HYDRAZINE(185456-26-2)
• EPA Substance Registry System: BOC3-HYDRAZINE(185456-26-2)

Safety Data

• Hazardous Substances Data: 185456-26-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
BOC3-HYDRAZINE is used as a reagent in organic synthesis for its ability to release hydrazine under specific reaction conditions, facilitating the formation of various organic compounds.
Used in Pharmaceutical and Agrochemical Preparation:
BOC3-HYDRAZINE is used as a building block in the preparation of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Polymer Crosslinking:
BOC3-HYDRAZINE is used as a crosslinking agent in the manufacturing of polymers, enhancing their properties and performance.
Used in Dye Production:
BOC3-HYDRAZINE is used in the production of dyes, contributing to the development of new colorants for various applications.
Used as a Chemical Intermediate:
BOC3-HYDRAZINE is used as a chemical intermediate in the synthesis of other compounds, enabling the production of a wide range of chemical products.
Used in Various Industries:
BOC3-HYDRAZINE is used across various industries due to its versatility and ability to release hydrazine, making it a valuable compound for numerous applications.

Upstream product

• 57699-88-4 1-tert-butoxycarbonyl-2-carbobenzyloxyhydrazine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 870-50-8 di-tert-butyl-diazodicarboxylate 
• 185456-24-0 C₂₃H₃₄N₂O₈ 

Downstream Products

• 185456-38-6 1-(2,4-dinitrophenyl)-1,2,2-tris(tert-butoxycarbonyl)hydrazine 
• 828246-96-4 N,N'-diacetyl-N'-(4-[1,3]dioxolan-2-yl-phenyl)-hydrazinecarboxylic acid tert-butyl ester 
• 828246-95-3 C₂₄H₃₆N₂O₈ 
• 185456-45-5 C₁₇H₂₅N₃O₆ 
• 185456-43-3 N-benzyl-N’-[(tert-butoxy)carbonyl](tert-butoxy)carbohydrazide 
• 185456-52-4 C₂₃H₂₇N₅O₁₀ 
• 312934-66-0 1,2-Bis(t-butyloxycarbonyl)-2-(4-methylphenyl)-1-phenylhydrazine 
• 65578-58-7 di-tert-butyl 1-phenylhydrazine-1,2-dicarboxylate 
• 828246-98-6 C₂₂H₃₂N₂O₇ 
• 828246-99-7 N,N'-diacetyl-N'-(4-formyl-phenyl)-hydrazinecarboxylic acid tert-butyl ester 
• 958001-24-6 benzyl 4-[N-tert-butoxycarbonyl-N-di(tert-butoxycarbonyl)-amino]amino-4-deoxy-2,3-O-isopropylidene-α-D-arabinopyranoside 

Relevant articles and documents

Addition of arylboronic acids to symmetrical and unsymmetrical azo compounds

(Chemical Equation Presented) The addition of aryl- and heteroarylboronic acids to azo compounds is described. Copper salt catalysis was necessary to perform the reaction under mild conditions and high yields. Excellent regioselectivity was observed in addition to unsymmetrical azo compounds.

Ein prototypisches Reagens fuer die Synthese substituierter Hydrazine

Keywords: Alkylierungen; Hydrazine; Phasentransferkatalyse; Schutzgruppen