N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane

N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane - Names and Identifiers

Name	N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane
Synonyms	3-BOC-AMINO-2-METHYL-PROPYLAMINE N-BOC-2-METHYL-1,3-DIAMINOPROPANE N-BOC-2-METHYL-1,3-PROPANEDIAMINE TERT-BUTYL N-(3-AMINO-2-METHYLPROPYL)CARBAMATE N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane N-(TERT-BUTOXYCARBONYL)-2-METHYL-1,3-PROPANEDIAMINE N-(TERT-BUTOXYCARBONYL)-2-METHYL-1,3-DIAMINOPROPANE N-(3-AMINO-2-METHYLPROPYL)CARBAMIC ACID TERT-BUTYL ESTER Carbamic acid, (3-amino-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)
CAS	480452-05-9

N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane - Physico-chemical Properties

Molecular Formula	C9H20N2O2
Molar Mass	188.27
Density	0.98
Boling Point	282.6±23.0 °C(Predicted)
pKa	12.65±0.46(Predicted)
Storage Condition	Keep in dark place,Inert atmosphere,Room temperature
Refractive Index	1.4560-1.4590

N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane - Risk and Safety

Hazard Symbols	Xn - Harmful
Risk Codes	22 - Harmful if swallowed

N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane - Introduction

N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane is an organic compound. The following is a detailed description of its nature, use, formulation and safety information:

Nature:
-Appearance: White crystal or crystalline powder
-Molecular formula: C11H24N2O2
-Molecular weight: 216.32g/mol
-Melting point: 80-82 degrees Celsius
-Boiling Point: No data available
-Solubility: Soluble in organic solvents, such as ether and alcohol, insoluble in water.

Use:
- N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane is a commonly used organic synthesis intermediate, which is widely used in the field of pharmaceutical synthesis and organic synthesis.
-It can be used as a protective group for synthetic polypeptides or peptide compounds.
-It can also be used to synthesize biologically active compounds, such as drugs and biomarkers.

Preparation Method:
- N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane preparation usually involves the following steps:
1.2-methyl-1,3-diaminopropane reacts with tert-butoxycarbonyl chloride to form N-(tert-butoxycarbonyl)-2-methyl-1, 3-diaminoppane under alkaline conditions.
2. The pure product is obtained by appropriate manipulation, such as crystallization or filtration.

Safety Information:
-specific hazard information of N-(tert-butoxycarbonyl)-2-methyl-1,3-diaminopropane has not been publicly reported.
-However, as an organic compound, it may be irritating to the skin, eyes and respiratory tract. Therefore, when handling and using, it is important to take appropriate safety measures, including wearing personal protective equipment, and operating in a well-ventilated environment.

Last Update：2024-04-09 20:48:19