62595-52-2

Basic information

• Product Name: 1-AMINO-10-UNDECENE
• Synonyms: TIMTEC-BB SBB008871;1-AMINO-10-UNDECENE;1-AMINO-10-UNDECENE, 97%,;undec-10-en-1-amine
• CAS NO: 62595-52-2
• Molecular Formula: C₁₁H₂₃N
• Molecular Weight: 169.31
• Mol File: 62595-52-2.mol
• Article Data: 13

Chemical Properties

• Melting Point: 85-86 °C
• Boiling Point: 238.999 °C at 760 mmHg
• Flash Point: 89.086 °C
• Appearance: /
• Density: 0.811 g/cm³
• Refractive Index: 1.4487
• PKA: 10.67±0.10(Predicted)
• CAS DataBase Reference: 1-AMINO-10-UNDECENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-AMINO-10-UNDECENE(62595-52-2)
• EPA Substance Registry System: 1-AMINO-10-UNDECENE(62595-52-2)

Safety Data

• Hazardous Substances Data: 62595-52-2(Hazardous Substances Data)

Usage

General Description

1-AMINO-10-UNDECENE is a chemical compound with the chemical formula C11H23N. It is an alkene amine, which means it contains a carbon-carbon double bond and an amino group. 1-AMINO-10-UNDECENE is used as a synthetic intermediate in the production of various chemicals, including surfactants, lubricants, and specialty chemicals. It has a long carbon chain, which makes it useful in applications where a long hydrophobic tail is desired, such as in the production of detergents and emulsifiers. Additionally, it can be used as a building block for the synthesis of pharmaceuticals and agricultural chemicals. Overall, 1-AMINO-10-UNDECENE is a versatile chemical that has a wide range of industrial applications.

Upstream product

• 505-95-3 12-hydroxydodecanoic acid 
• 112-43-6 10-Undecen-1-ol 
• 7766-50-9 1-undecen-11-ylbromide 

Downstream Products

• 463930-53-2 tert-butyl N-(11-bromoundecyl)carbamate 
• 53179-04-7 undec-10-enenitrile 
• 116821-45-5 11-(amino)undecyltriethoxysilane 
• 88124-95-2 2-(undec-10-en-1-yl)isoindoline-1,3-dione 
• 1242054-47-2 C₃₃H₄₇NO₄ 
• 1246518-39-7 N₆-[(benzyloxy)carbonyl]-N₁-(10-undecenoyl)-L-lysyl-N-(10-undecenyl)-amide 
• 1228757-77-4 C₅₄H₈₆N₄O₆ 
• 1096563-78-8 C₄₅H₆₃F₃N₆O₅Si 

Relevant articles and documents

Siloxanes with pendent naphthalene diimides: Synthesis and fluorescence quenching

Cyclic siloxanes with pendent naphthalene diimide groups were synthesized via hydrosilylation to form amorphous electron-accepting compounds. Photophysical measurements and >99.9% fluorescence quenching of well-known p-type polymers by the siloxanes demonstrate that these siloxanes form a new class of highly efficient n-type materials that provide some control over intermolecular interactions.

Bio-based α,ω-Functionalized Hydrocarbons from Multi-step Reaction Sequences with Bio- and Metallo-catalysts Based on the Fatty Acid Decarboxylase OleTJE

OleT from Jeotgalicoccus sp. ATCC 8456 catalyzes the decarboxylation of ω-functionalized fatty acids to the corresponding alkenols, which can themselves serve as starting material for the synthesis of polymers and fine chemicals. To show the versatility of possible reactions, a series of in vitro reaction cascades was developed where an alkenol produced by the decarboxylation of ω-hydroxy fatty acids can be further converted into alkenylamines and diols. By coupling OleT with an alcohol dehydrogenase or alcohol oxidase as well as an amino-transaminase, an oxidative decarboxylation followed by the oxidation of the terminal alcohol and a subsequent reductive transamination could be carried out. By using different cofactors or electron sources, the reactions could be performed sequentially or simultaneously. The combination of enzymatic decarboxylation with a ruthenium catalyst in a chemo-enzymatic cascade provides a novel way to synthesize long-chain diols.

ARYL, HETEROARYL, AND HETEROCYCLIC COMPOUNDS FOR TREATMENT OF MEDICAL DISORDERS

Compounds, methods of use, and processes for making inhibitors of complement Factor D comprising Formula I, or a pharmaceutically acceptable salt or composition thereof wherein R12 or R13 on the A group is an aryl, heteroaryl or heterocycle (R32) are provided. The inhibitors of Factor D described herein reduce the excessive activation of complement.