N-(1,4-dihydroxybutan-2-yl)carbamic acid tert-butyl ester - Names and Identifiers
Name | (R)-(+)-2-(Boc-Amino)-1,4-butanediol
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Synonyms | (R)-2-Boc-amino-butane-1,4-diol (R)-(+)-2-(Boc-Amino)-1,4-butanediol (R)-(+)-2-(Boc-Amino)-1,4-Butanediol -tert-Butyl (1,4-dihydroxybutan-2-yl) (2R)-(tert-Butoxycarbonylamino)butane-1,4-diol (R)-TERT-BUTYL 1,4-DIHYDROXYBUTAN-2-YLCARBAMATE tert-butyl [(2R)-1,4-dihydroxybutan-2-yl]carbamate N-(1,4-dihydroxybutan-2-yl)carbamic acid tert-butyl ester [(1R)-3-Hydroxy-1-(hydroxymethyl)propyl]carbamic acid tert-butyl ester [(1R)-3-Hydroxy-1-(hydroxymethyl)propyl]carbamic acid tert-butyl ester Carbamic acid, [(1R)-3-hydroxy-1-(hydroxymethyl)propyl]-, 1,1-dimethylethyl
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CAS | 397246-14-9
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EINECS | 210-006-7 |
InChI | InChI=1/C9H19NO4/c1-9(2,3)14-8(13)10-7(6-12)4-5-11/h7,11-12H,4-6H2,1-3H3,(H,10,13)/t7-/m1/s1 |
N-(1,4-dihydroxybutan-2-yl)carbamic acid tert-butyl ester - Physico-chemical Properties
Molecular Formula | C9H19NO4
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Molar Mass | 205.25 |
Density | 1.110 |
Melting Point | 64-68 °C |
Boling Point | 365.0±32.0 °C(Predicted) |
Flash Point | 174.571°C |
Vapor Presure | 0mmHg at 25°C |
Appearance | Crystalline Powder |
Color | White |
pKa | 11.81±0.46(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.476 |
MDL | MFCD08703679 |
N-(1,4-dihydroxybutan-2-yl)carbamic acid tert-butyl ester - Introduction
(R)-( )-2-(Boc-Amino)-1,4-butanediol, also known as (R)-( )-2-(Boc-Amino)-1,4-butanediol, is an organic compound, commonly known by the abbreviation (R)-( )-Boc-Amino-Butanediol. It has a molecular formula of C10H21NO4 and a molecular weight of 219.28g/mol.
Nature:
(R)-( )-2-(Boc-Amino)-1,4-butanediol is a solid with a white to almost white color. It has the property of being soluble in polar solvents, such as alcohols and esters, and insoluble in non-polar solvents. The compound has optical activity, optical rotation, optical rotation is [α]25D = 16 °. It is a chiral molecule with two stereocenters.
Use:
(R)-( )-2-(Boc-Amino)-1,4-butanediol is widely used as a reagent or intermediate in organic synthesis. Its main applications include drug synthesis, ligand synthesis, and chiral control in organic synthesis. As a chiral building block, it can be used in the synthesis of chiral drugs, ligands and chiral polymer materials.
Preparation Method:
(R)-( )-2-(Boc-Amino)-1,4-butanediol is usually prepared by reacting (R)-( )-2-amino -1,4-butanediol with N-tert-butoxycarbonylimine. This reaction is generally carried out under neutral or basic conditions, and the product obtained after the reaction can be purified by crystallization.
Safety Information:
The best way to confirm the safe use and handling of compounds is to consult the relevant chemical literature and follow proper laboratory procedures. In general, handle and store compounds properly, avoiding contact with eyes, skin, and inhalation. If contact occurs, rinse immediately with plenty of water. Also, work in a well-ventilated environment and wear appropriate protective equipment, including laboratory gloves and goggles.
Last Update:2024-04-09 21:32:40