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 Detail:
Supply with High Purity and Stable Quality
High Quality, Commercial Production
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.
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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