116407-32-0

Basic information

• Product Name: (1R,2R)-1,2-Diaminocyclohexane D-tartrate
• Synonyms: (1R,2R)-1,2-Diaminocyclohexane D-tartrate;(1R,2R)-Cyclohexane-1,2-diaMine (2S,3S)-2,3-dihydroxysuccinate
• CAS NO: 116407-32-0
• Molecular Formula: C₄H₆O₆*C₆H₁₄N₂
• Molecular Weight: 264.2756
• Mol File: 116407-32-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Room temperature.
• CAS DataBase Reference: (1R,2R)-1,2-Diaminocyclohexane D-tartrate(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-1,2-Diaminocyclohexane D-tartrate(116407-32-0)
• EPA Substance Registry System: (1R,2R)-1,2-Diaminocyclohexane D-tartrate(116407-32-0)

Safety Data

• Hazardous Substances Data: 116407-32-0(Hazardous Substances Data)

Usage

Uses

(1R,2R)-1,2-Diaminocyclohexane D-Tartrate is a reagent in the synthesis of polyimides containing a chiral diimine.

Upstream product

• 147-71-7 D-tartaric acid 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 

Downstream Products

• 284497-48-9 N,N'-(1R,2R)-cyclohexane-1,2-diyl-bis-[1-(pyridine-2-yl)methanimine] 
• 284497-27-4 (1R,2R)-N,N'-bis(6-methyl-2-pyridylmethylidene)-1,2-cyclohexyldiimine 
• 1598408-97-9 (R,R)-N¹,N²-bis((5-methylfuran-2-yl)methyl)cyclohexane-1,2-diamine 
• 1598408-94-6 (1R,2R)-N,N′-bis[(5-methylfuran-2-yl)methylidene]cyclohexane-1,2-diamine 
• 1610762-32-7 (R,R)-N,N′-bis(5-methylthiophen-2-ylmethyl)cyclohexane-1,2-diamine 
• 857256-24-7 (1R,2R)-N,N'-bis(2-nitrophenyl)cyclohexane-1,2-diamine 
• 951153-76-7 N,N′-((1R,2R)-cyclohexane-1,2-diyl)bis(benzene-1,2-diamine) 
• 182368-90-7 (R,R)-N,N'-bis(3-tert-butyl-5-methylsalicylidene)-1,2-cyclohexanediamine 
• 98795-02-9 (R,R)-N,N'-bis(2-hydroxy-3-tert-butyl-benzylidene)-1,2-diaminocyclohexane 

Relevant articles and documents

Preparation method and application of trans-cyclohexanediamine tartrate

The invention provides a preparation method of trans-cyclohexanediamine tartrate. The preparation method comprises the steps of charging, dropwise adding of trans-cyclohexanediamine, dropwise adding of glacial acetic acid, heat-insulation reaction and cooling. The invention further provides application of the trans-cyclohexanediamine tartrate in preparation of a schiff base metallic cobalt complex. The specific rotation of the prepared trans-cyclohexanediamine tartrate is minus 11 degrees to minus 13 degrees, the content is greater than or equal to 98.0%, and the appearance of the trans-cyclohexanediamine tartrate is off-white or light yellow crystal. The yield of the prepared trans-cyclohexanediamine tartrate is 55.8-56%; and reaction conditions are mild, and the preparation method is simple to operate, is carried out under normal pressure, and is high in safety.