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Personlized Products (R)-Glycidyl 3-Nitrobenzenesulfonate - (±)-trans-1,2-Diaminocyclohexane CAS 1121-22-8 Purity ≥98.0% High Purity – Ruifu Featured Image
  • Personlized Products (R)-Glycidyl 3-Nitrobenzenesulfonate - (±)-trans-1,2-Diaminocyclohexane CAS 1121-22-8 Purity ≥98.0% High Purity – Ruifu

Personlized Products (R)-Glycidyl 3-Nitrobenzenesulfonate - (±)-trans-1,2-Diaminocyclohexane CAS 1121-22-8 Purity ≥98.0% High Purity – Ruifu

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Personlized Products (R)-Glycidyl 3-Nitrobenzenesulfonate - (±)-trans-1,2-Diaminocyclohexane CAS 1121-22-8 Purity ≥98.0% High Purity – Ruifu Detail:

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Chemical Name (±)-trans-1,2-Diaminocyclohexane
Synonyms trans-1,2-Diaminocyclohexane; trans-1,2-Cyclohexanediamine
CAS Number 1121-22-8
CAT Number RF-CC281
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C6H14N2
Molecular Weight 114.19
Melting Point 14.0-15.0℃ (lit.)
Boiling Point  79.0-81.0℃/15 mmHg (lit.)
Density 0.951 g/mL at 25℃ (lit.)
Refractive Index n20/D 1.489 (lit.)
Solubility Soluble in Water
Sensitivity  Air Sensitive, Hygroscopic
Shipping Condition Shipped Under Ambient Temperature
Brand Ruifu Chemical
Item Specifications
Appearance Colorless or Yellowish Liquid
Purity ≥98.0% (GC)
Water ≤1.0%
Test Standard Enterprise Standard
Usage Chiral Compounds; Pharmaceutical Intermediates

Package: Bottle, 25kg/Barrel, or according to customer’s requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

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Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (±)-trans-1,2-Diaminocyclohexane (CAS: 1121-22-8) with high quality.

(±)-trans-1,2-Diaminocyclohexane (CAS: 1121-22-8) is an organic compound with the formula C6H10(NH2)2. This diamine is a building block for C2-symmetric ligands that are useful in asymmetric catalysis.

(±)-trans-1,2-Diaminocyclohexane (CAS: 1121-22-8) is employed in the synthesis of macrocyclic [3+3] hexa Schiff base. It also plays an important role in the preparation of multidentate ligands, chiral auxiliaries and chiral stationary phases. Further, it is used to prepare [2+2] macrocyclization by reacting with aliphatic dialdehydes. In addition to this, it acts as a chiral ligand, which finds application in asymmetric catalysis.

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