1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE
1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE
CAS: 137731-41-0
Molecular Formula: C11H22N2O2
1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE - Names and Identifiers
| Name | 1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE |
| Synonyms | N-Boc-trans-1,2-cyclohexanediamine N-BOC-TRANS-1,2-DIAMINOCYCLOHEXANE Trans-N-Boc-1,2-Cyclohexanediamine TRANS-N-BOC-1,2-DIAMINOCYCLOHEXANE N-Boc-trans-1,2-diamino-cyclohexane 1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE 1-N-BOC-1(R), 2(R)-CYCLOHEXYLDIAMINE tert-butyl [(1R,2R)-2-aminocyclohexyl]carbamate trans-(2-Amino-cyclohexyl)-carbamic acid tert-butyl ester Carbamic acid, N-[(1R,2R)-2-aminocyclohexyl]-, 1,1-dimethylethyl ester, rel- |
| CAS | 137731-41-0 |
| 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)/t8-,9-/m1/s1 |
1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE - Physico-chemical Properties
| Molecular Formula | C11H22N2O2 |
| Molar Mass | 214.3 |
| Density | 1.02±0.1 g/cm3(Predicted) |
| Boling Point | 322.1±31.0 °C(Predicted) |
| Flash Point | 148.6°C |
| Vapor Presure | 0.000286mmHg at 25°C |
| pKa | 12.26±0.40(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
| Refractive Index | 1.488 |
1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 3259 |
| Hazard Class | IRRITANT |
1-N-BOC-1,2-TRANS-CYCLOHEXYLDIAMINE - Introduction
N-tert-butoxycarbonyl-trans-1, 2-cyclohexanediamine (abbreviated tBOC-1,2-cyclohexanediamine) is an organic compound. Its chemical formula is C11H21NO2 and its molecular weight is 199.29g/mol. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
- tBOC-1, 2-cyclohexanediamine is a solid crystal with a white or off-white appearance.
-It is stable at room temperature, but may decompose at high temperatures. The
- tBOC group can be easily deprotected under basic conditions, thereby reducing to 1,2-cyclohexanediamine.
Use:
- tBOC-1, 2-cyclohexanediamine is an important organic synthesis intermediate, which is widely used in the fields of medicine and chemical industry.
-It can be used for the synthesis of peptides, drug molecules and other organic compounds.
-It can also be used as a skeleton molecule to build complex organic molecules.
Preparation Method:
- tBOC-1, the preparation of 2-cyclohexanediamine can be achieved by a variety of methods. The more commonly used method is to react 1,2-cyclohexanediamine with t-tert-butoxycarbonyl chloride (BOC-Cl) under alkaline conditions.
-The reaction is generally carried out at room temperature, and after the completion of the reaction, it is treated with acid to remove the remaining protecting group.
Safety Information:
- tBOC-1, 2-cyclohexanediamine is less toxic, but general laboratory safety procedures should still be followed.
-Avoid inhalation, ingestion or contact with skin and eyes during operation.
-Waste disposal shall comply with local regulatory standards.
Please note that any operations in chemical experiments should be carried out under suitable laboratory conditions and follow relevant safety operating guidelines and regulations.
Nature:
- tBOC-1, 2-cyclohexanediamine is a solid crystal with a white or off-white appearance.
-It is stable at room temperature, but may decompose at high temperatures. The
- tBOC group can be easily deprotected under basic conditions, thereby reducing to 1,2-cyclohexanediamine.
Use:
- tBOC-1, 2-cyclohexanediamine is an important organic synthesis intermediate, which is widely used in the fields of medicine and chemical industry.
-It can be used for the synthesis of peptides, drug molecules and other organic compounds.
-It can also be used as a skeleton molecule to build complex organic molecules.
Preparation Method:
- tBOC-1, the preparation of 2-cyclohexanediamine can be achieved by a variety of methods. The more commonly used method is to react 1,2-cyclohexanediamine with t-tert-butoxycarbonyl chloride (BOC-Cl) under alkaline conditions.
-The reaction is generally carried out at room temperature, and after the completion of the reaction, it is treated with acid to remove the remaining protecting group.
Safety Information:
- tBOC-1, 2-cyclohexanediamine is less toxic, but general laboratory safety procedures should still be followed.
-Avoid inhalation, ingestion or contact with skin and eyes during operation.
-Waste disposal shall comply with local regulatory standards.
Please note that any operations in chemical experiments should be carried out under suitable laboratory conditions and follow relevant safety operating guidelines and regulations.
Last Update：2024-04-09 15:17:52
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