trans-1,4-Diaminocyclohexane, N1-BOC protected

trans-1,4-Diaminocyclohexane, N1-BOC protected - Names and Identifiers

Name	N-Boc-1,4-cyclohexanediamine
Synonyms	Boc-1,4-trans-DACH*HCl N-Boc-1,4-cyclohexanediamine N-BOC-1,4-DIAMINECYCLOHEXANE 1-N-BOC-1,4-CYCLOHEXANEDIAMINE BUTYL 4-AMINOCYCLOHEXYLCARBAMATE Trans-N-box-1,4-cyclohexanediamine 1-BOC-AMINO-1,4-CYCLOHEXANEDIAMINE tert-butyl (4-aminocyclohexyl)carbamate tert-butyl N-(4-aminocyclohexyl)carbamate trans-1,4-Diaminocyclohexane, N1-BOC protected 4-[(tert-butoxycarbonyl)amino]cyclohexanaminium (4-AMINO-CYCLOHEXYL)-CARBAMIC ACID TERT-BUTYL ESTER
CAS	195314-59-1
InChI	InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h8-9H,4-7,12H2,1-3H3,(H,13,14)/t8-,9+

trans-1,4-Diaminocyclohexane, N1-BOC protected - 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
Appearance	Solid
Color	White
pKa	12.44±0.40(Predicted)
Storage Condition	Keep in dark place,Inert atmosphere,Room temperature
Refractive Index	1.488

trans-1,4-Diaminocyclohexane, N1-BOC protected - Risk and Safety

Risk Codes	51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Safety Description	61 - Avoid release to the environment. Refer to special instructions / safety data sheets.
UN IDs	UN 3077 9 / PGIII
WGK Germany	3
HS Code	29225090
Hazard Class	8

trans-1,4-Diaminocyclohexane, N1-BOC protected - Introduction

N-Boc-1,4-cyclohexanediamine(N-Boc-1) is an organic compound containing a cyclohexane ring and two amine groups in its structure. Its chemical formula is C10H20N2O2.

N-Boc-1,4-cyclohexanediamine has the following properties:
1. Appearance: colorless to light yellow crystal;
2. Melting Point: about 66-70 ° C;
3. Solubility: Soluble in some organic solvents, such as ethanol, dimethylformamide, etc.

N-Boc-1, one of the main uses of 4-cyclohexanediamine is as a synthetic intermediate. It can be used to synthesize some drugs, dyes, coatings and polymer materials. In addition, it can also be used to synthesize other organic compounds, such as biologically active compounds.

The method for preparing N-Boc-1,4-cyclohexanediamine can be obtained by reacting cyclohexanedione and N-Boc protected 1,4-diamine. The specific reaction conditions can be adjusted according to the experimental requirements.

When using or handling N-Boc-1,4-cyclohexanediamine, you need to pay attention to the following safety information:
1. It can cause irritation to the eyes, skin and respiratory system, so protective glasses, gloves and respiratory protective equipment must be worn;
2. Avoid direct contact and inhalation, and operate under well-ventilated conditions;
3. Should be stored away from the fire and oxidant, storage temperature should generally be lower than room temperature.

Please note that when conducting chemical experiments or using chemicals, be sure to follow the relevant safety operating procedures and operate after understanding and mastering sufficient professional knowledge.

Last Update：2024-04-09 20:49:11