317595-54-3

Basic information

• Product Name: N-Boc-1,2-Diaminocyclohexane
• Synonyms: 1-AMINO-2-(BOC-AMINO)CYCLOHEXANE;1-N-BOC-AMINO-1,2-CYCLOHEXANEDIAMINE;Carbamic acid, (2-aminocyclohexyl)-, 1,1-dimethylethyl ester (9CI);1-N-Boc-Amino-1,2-cyclohexaned;1-N-Boc-1,2-Cyclohexyldiamino;N-BOC-1,2-DIAMINOCYCLOHEXANE;Carbamic acid, N-(2-aminocyclohexyl)-, 1,1-dimethylethyl ester;N-Boc-trans-1
• CAS NO: 317595-54-3
• Molecular Formula: C₁₁H₂₂N₂O₂
• Molecular Weight: 214.3
• Product Categories: N-BOC;pharmacetical
• Mol File: 317595-54-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 322.1 °C at 760 mmHg
• Flash Point: 148.6 °C
• Appearance: /
• Density: 1.02 g/cm³
• Vapor Pressure: 0.000286mmHg at 25°C
• Refractive Index: 1.488
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 12.26±0.40(Predicted)
• CAS DataBase Reference: N-Boc-1,2-Diaminocyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: N-Boc-1,2-Diaminocyclohexane(317595-54-3)
• EPA Substance Registry System: N-Boc-1,2-Diaminocyclohexane(317595-54-3)

Safety Data

• Hazardous Substances Data: 317595-54-3(Hazardous Substances Data)

Usage

General Description

N-Boc-1,2-Diaminocyclohexane is a chemical compound with the formula C12H24N2O2. It is a derivative of cyclohexane with two amino groups and a Boc (tert-butoxycarbonyl) protecting group. N-Boc-1,2-Diaminocyclohexane is commonly used as a building block in organic synthesis and pharmaceutical research. It can be used in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and materials. N-Boc-1,2-Diaminocyclohexane is also known for its potential application in the field of asymmetric catalysis as a chiral building block. Additionally, it is used as a ligand in metal-catalyzed reactions, and its versatile reactivity makes it a valuable tool in chemical research and development.

InChI:InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8(9)12/h8-9H,4-7,12H2,1-3H3,(H,13,14)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 694-83-7 rac-diaminocyclohexane 
• 1436-59-5 cis-cyclohexane-1,2-diamine 
• 21436-03-3 (S,S)-1,2-diaminocyclohexane 

Downstream Products

• 554-68-7 triethylamine hydrochloride 
• 1300730-77-1 ethyl 2-(4-(3-(2-(tert-butoxycarbonylamino)cyclohexyl)ureido)-2-chlorophenyl)acetate 
• 1416225-79-0 C₂₁H₃₂N₂O₂ 
• 1416225-80-3 C₁₈H₂₅BrN₂O₂ 
• 1416304-83-0 C₂₁H₂₈N₂ 
• 1416304-84-1 C₂₁H₂₈N₂ 
• 1416304-85-2 C₂₁H₂₈N₂ 
• 1416304-86-3 C₂₂H₃₀N₂ 
• 1416304-87-4 C₂₃H₃₂N₂ 
• 1416304-88-5 C₂₃H₃₂N₂ 
• 1416304-89-6 C₂₄H₃₄N₂ 
• 1416304-90-9 C₂₄H₃₄N₂ 
• 1416304-91-0 C₂₂H₃₀N₂ 
• 1416304-92-1 C₂₀H₂₅ClN₂ 

Relevant articles and documents

Characteristics of gelation by amides based on trans-1,2-diaminocyclohexane: The importance of different substituents

Six diamides were prepared from trans-(1R,2R)-1,2-diaminocyclohexane and the corresponding racemate and were subsequently used as gelators. Three chiral compounds and their racemates were prepared. One of the chiral compounds and its racemate contained tw

Synthesis and antitubercular activity evaluation of novel unsymmetrical cyclohexane-1,2-diamine derivatives

A library of unsymmetrical cyclohexane-1,2-diamine derivatives were synthesized and evaluated for their activity against Mycobacterium tuberculosis H37Rv in vitro. Out of the 46 compounds synthesized, eight compounds (11h, 13a, 13e, 13f, 14a, 14c, 14d, an

Cyclohexyl-triethylenetetraamine hexacetic acid

The present invention relates to new rigid chelating structures, to methods for preparing these materials, and to their use in preparing radiometal labeled immunoconjugates. These new chelates include cyclohexyl EDTA monohydride, the trans forms of cyclohexyl DTPA and TTHA, and derivatives of these cyclohexyl polyaminocarboxylate materials.