894493-95-9

Basic information

• Product Name: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine
• Synonyms: (1S,2S)-(+)-N,N-Dimethyl diaminocyclohexane;(1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine;(1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine;(1S,2S)-N,N-Dimethyl-1,2-cyclohexanediamine;1R,2R-(-)-OR1S,2S-(+)-N,N-DIAMINOCYCLOHEXANE;N,N'-Dimethyl-1S,2S-Diaminocyclohexane;(1S,2S)-1-N,1-N-diMethylcyclohexane-1,2-diaMine;1S,2S-(+)-N,N-diaminocyclohexane
• CAS NO: 894493-95-9
• Molecular Formula: C₈H₁₈N₂
• Molecular Weight: 142.24
• Mol File: 894493-95-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 180 °C
• Flash Point: 62 °C
• Appearance: /
• Density: 0.92
• Refractive Index: 1.49
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 10.52±0.70(Predicted)
• CAS DataBase Reference: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine(894493-95-9)
• EPA Substance Registry System: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine(894493-95-9)

Safety Data

• Statements: 22-34
• Safety Statements: 26-36/37/39-45
• RIDADR: 2735
• HazardClass: 8
• PackingGroup: Ⅲ
• Hazardous Substances Data: 894493-95-9(Hazardous Substances Data)

Usage

Chemical Properties

Colorless liquid

InChI:InChI=1/C8H18N2/c1-10(2)8-6-4-3-5-7(8)9/h7-8H,3-6,9H2,1-2H3/t7-,8-/m0/s1

Upstream product

• 286-18-0 7-azabicyclo[4.1.0]heptane 
• 931-15-7 (1S,2S)-trans-2-aminocyclohexanol 
• 620597-07-1 N,N-dimethyl-N'-benzyl-1,2-cyclohexanediamine 
• 124-63-0 methanesulfonyl chloride 
• 100-46-9 benzylamine 

Downstream Products

• 1384718-12-0 1-((1R,2R)-2-aminocyclohexyl)-3-((1S,2S)-2-(dimethyl amino)cyclohexyl)thiourea 
• 1165796-68-8 C₂₄H₄₁N₃O₂S 
• 1165796-67-7 C₁₃H₂₇N₃O₂S 
• 1133834-56-6 C₃₅H₅₃N₃O₁₇S 
• 1133834-55-5 C₃₅H₅₃N₃O₁₇S 
• 1133834-54-4 C₂₃H₃₇N₃O₉S 
• 621-84-1 O-benzyl carbamate 
• 620960-26-1 1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-(dimethylamino)cyclohexyl]thiourea 
• 1373404-83-1 N-((1S,2S)-2-(3-((1S,2S)-2-(dimethylamino)cyclohexyl)thioureido)cyclohexyl)-1,1,1-trifluoromethanesulfonamide 

Relevant articles and documents

Preparation of C 2-Symmetric Biaryl Bisiminium Salts and Their Use as Organocatalysts for Asymmetric Epoxidation

Two C 2-symmetric bisiminium salt species containing biphenylazepinium units and derived from two chiral diamines were prepared and tested as organocatalysts for asymmetric epoxidation.

Asymmetric isomerization of ω-hydroxy-α,β-unsaturated thioesters into β-mercaptolactones by a bifunctional aminothiourea catalyst

We present a novel methodology for the asymmetric synthesis of β-mercaptolactones via isomerization of ω-hydroxy-α,β- unsaturated thioesters by means of a bifunctional aminothiourea catalyst. The catalyst interacts with the substrate through the cooperati

Analgesic N-[2-(furyl-methylamino and 2-thienylmethylamino)cycloaliphatic]be

Cis - and trans-N-(2-aminocycycloaliphatic)benzamide compounds of the formula STR1 e.g., N-methyl-N-[2-[(2-furylmethyl)methylamino]-cyclohexyl]-3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm-blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.