dicyclohexylamine (S)-2,3-bis(tert-butoxycarbonylamino)propanoate - Names and Identifiers
Name | N-[(tert-Butoxy)carbonyl]-3-[[(tert-Butoxy)carbonyl]amino]-L-alanine compd. with N-cyclohexylcyclohexanamine
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Synonyms | Boc-Dap(Boc)-OH·DCHA BOC-DAP(BOC)-OH DCHA Boc-L-Dap(Boc)-OH. DCHA boc-dap(boc)-oh dicyclohexylamine salt Boc-Dap(Boc)-OH (dicyclohexylammonium) salt N-α,N-β-di-Boc-L-2,3-diaminopropionic acid dicyc N-α,N-β-di-Boc-L-2,3-diaminopropionic acid dicyclohexylamine salt dicyclohexylamine (S)-2,3-bis(tert-butoxycarbonylamino)propanoate Boc-Dap(Boc)-OH·DCHA(Na,N3-diBoc-2,3-DiaMinopropionic acid dicyclohexylaMine salt ) Boc-Dap(Boc)-OH·DCHA N-α,N-β-di-Boc-L-2,3-diaMinopropionic acid dicyclohexylaMine salt N-[(tert-Butoxy)carbonyl]-3-[[(tert-Butoxy)carbonyl]amino]-L-alanine compd. with N-cyclohexylcyclohexanamine Nα,Nβ-Di-Boc-L-2,3-diaminopropionic acid (dicyclohexylammonium) salt, Boc-3-(Boc-amino)-L-alanine (dicyclohexylammonium) salt, Nα,Nβ-di-Boc-L-2,3-diaminopropionic acid (dicyclohexylammonium) salt
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CAS | 201472-68-6
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EINECS | 1533716-785-6 |
InChI | InChI=1/C13H24N2O6.C12H23N/c1-12(2,3)20-10(18)14-7-8(9(16)17)15-11(19)21-13(4,5)6;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h8H,7H2,1-6H3,(H,14,18)(H,15,19)(H,16,17);11-13H,1-10H2/t8-;/m0./s1 |
dicyclohexylamine (S)-2,3-bis(tert-butoxycarbonylamino)propanoate - Physico-chemical Properties
Molecular Formula | C25H47N3O6
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Molar Mass | 485.66 |
Boling Point | 634.6°C at 760 mmHg |
Flash Point | 337.6°C |
Vapor Presure | 9.75E-18mmHg at 25°C |
Storage Condition | Sealed in dry,Room Temperature |
dicyclohexylamine (S)-2,3-bis(tert-butoxycarbonylamino)propanoate - Risk and Safety
WGK Germany | 3 |
HS Code | 29242990 |
dicyclohexylamine (S)-2,3-bis(tert-butoxycarbonylamino)propanoate - Introduction
N-[tert-butoxycarbonyl]-3-[[tert-butoxycarbonyl] amino]-L-alanine and N-cyclohexylcyclohexylamine are two different compounds, their nature, use, formulation and safety information are described below:
N-[tert-butoxycarbonyl]-3-[[tert-butoxycarbonyl] amino]-L-alanine, also known as T-BOC-γ-aminobutyric acid, is an important organic compound. Specific properties are as follows:
-Appearance: Usually white crystals or crystalline powder.
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide or dichloromethane.
-Melting point: About 80-85 ° C.
The main use of this compound is as a protecting group in organic synthesis. It can form a stable t-BOC protection group by protecting the carbonyl group to prevent unwanted reaction of the specific group during the reaction. t-BOC protecting groups can be removed by acid-catalyzed or hydrogenative reduction as needed.
The method for preparing N-[tert-butoxycarbonyl]-3-[[tert-butoxycarbonyl] amino]-L-alanine involves reacting a t-BOC protected amino group with L-alanine.
Regarding safety information, N-[tert-butoxycarbonyl]-3-[[tert-butoxycarbonyl] amino]-L-alanine is generally considered to be relatively safe, but still need to pay attention to the following matters:
-Wear appropriate protective measures such as lab gloves and eye protection during operation.
-Avoid inhalation or contact with skin, if there is contact, rinse with plenty of water.
-Avoid contact with oxidants during storage and keep them in a dry, cool place.
N-cyclohexyl cyclohexylamine is an organic compound with specific properties as follows:
-Appearance: Usually colorless to light yellow liquid.
-Odor: Special ammonia smell.
-Density: about 0.941 g/mL.
-Boiling point: About 156-158 ° C.
N-Cyclohexylcyclohexylamine is mainly used as solvent, catalyst and intermediate. It can be used in organic synthesis to synthesize a variety of organic compounds, such as polyurethane, dyes, rubber and plastics.
The method for preparing N-cyclohexyl cyclohexylamine mainly involves reacting cyclohexanone with ammonia.
For safety information, N-cyclohexyl cyclohexylamine requires the following:
-Wear appropriate protection, such as lab gloves and eye protection.
-Avoid inhalation or contact with skin, if there is contact, rinse with plenty of water.
-Keep away from open flames or high temperature sources during use to prevent explosion or combustion.
Please note that before conducting any chemical experiments or applying chemicals, you should carefully read and follow the relevant safety practices and follow the correct operating procedures.
Last Update:2024-04-09 20:02:46