Boc-D-b-Leucine
boc-l-beta-homovaline
CAS: 183990-64-9
Molecular Formula: C11H21NO4
Boc-D-b-Leucine - Names and Identifiers
| Name | boc-l-beta-homovaline |
| Synonyms | Boc-β-HoVal-OH Boc-D-b-Leucine boc-beta-leu-oh Boc-D-β-HoVal-OH boc-val-(c*ch2)oh boc-d-beta-leu-oh Boc-beta-HoVal-OH boc-beta-homovaline boc-beta-homoval-oh Boc-(R)-beta-hoMo-Val boc-l-beta-homovaline BOC-L-BETA-HOMOVALINE L-beta-Leucine, N-Boc protected N-t-butoxycarbonyl-l-beta-homovaline (r)-3-(boc-amino)-4-methylpentanoic acid (R)-N-Boc-3-Amino-4-methylpentanoic Acid (r)-n-boc-3-amino-4-methylpentanoic acid (r)-3-(t-butoxycarbonyl-amino)-4-methylpentanoic acid (3R)-3-[(tert-butoxycarbonyl)amino]-4-methylpentanoic acid (3R)-3-{[(tert-butoxy)carbonyl]amino}-4-methylpentanoic acid |
| CAS | 183990-64-9 |
| InChI | InChI=1/C11H21NO4/c1-7(2)8(6-9(13)14)12-10(15)16-11(3,4)5/h7-8H,6H2,1-5H3,(H,12,15)(H,13,14)/t8-/m1/s1 |
| InChIKey | LUXMZCJCTUATDM-MRVPVSSYSA-N |
Boc-D-b-Leucine - Physico-chemical Properties
| Molecular Formula | C11H21NO4 |
| Molar Mass | 231.29 |
| Density | 1.061 |
| Melting Point | 115-120℃ |
| Boling Point | 360.4±25.0 °C(Predicted) |
| Flash Point | 171.8°C |
| Vapor Presure | 3.59E-06mmHg at 25°C |
| Appearance | Solid |
| BRN | 7568192 |
| pKa | 4.45±0.10(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.461 |
| Physical and Chemical Properties | Storage Conditions: Store at 0-5 ℃ WGK Germany:3 |
Boc-D-b-Leucine - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| Hazard Class | IRRITANT |
Boc-D-b-Leucine - Introduction
R-N-tert-butoxycarbonyl -3-amino -4-methyl pentanoic acid hydrochloride (R-N-Boc-3-amino -4-methyl pentanoic acid ester hydrochloride) is an organic compound, its properties, uses, the legal and safety information is as follows:
Nature:
-molecular formula: C15H27NO5 · HCl
-Molecular weight: 345.85g/mol
-Appearance: White crystalline solid
-Melting point: about 130-134 ° C
-Solubility: Slightly soluble in water, easily soluble in organic solvents such as ethanol and dimethylformamide
Use:
R-N-Boc-3-amino -4-methyl valerate hydrochloride is commonly used as a pharmaceutical intermediate and organic synthetic compound. It can be used as a protecting group during synthesis to protect an amino group or a hydroxyl group, while a deprotection reaction can be performed under appropriate conditions to obtain a target compound. The compounds are widely used in the preparation of pharmaceuticals, dyes, pesticides and other organic compounds.
Method:
The method of preparing R-N-Boc-3-amino -4-methyl valerate hydrochloride usually involves the following steps:
1. Reaction of 3-amino-4-methylpentanoic acid with the R-enantiomer of tert-butyryl chloride (tert-butyryl chloride) yields tert-butyl R-N-Boc-3-amino-4-methylpentanoate.
2. The product is reacted with hydrochloric acid to obtain R-N-Boc-3-amino-4-methylvalerate hydrochloride.
Safety Information:
R-N-Boc-3-amino -4-methyl valerate hydrochloride is less toxic and corrosive under normal operating conditions. However, as an organic compound, appropriate laboratory safety measures should be taken, including wearing appropriate protective gloves and eye protection to avoid skin contact and inhalation. If necessary, it should be operated in a well-ventilated environment and stored in a sealed container, away from fire and oxidizing agents. When handling this compound, it is recommended to refer to the relevant safety Data Sheet (MSDS) for more detailed information.
Nature:
-molecular formula: C15H27NO5 · HCl
-Molecular weight: 345.85g/mol
-Appearance: White crystalline solid
-Melting point: about 130-134 ° C
-Solubility: Slightly soluble in water, easily soluble in organic solvents such as ethanol and dimethylformamide
Use:
R-N-Boc-3-amino -4-methyl valerate hydrochloride is commonly used as a pharmaceutical intermediate and organic synthetic compound. It can be used as a protecting group during synthesis to protect an amino group or a hydroxyl group, while a deprotection reaction can be performed under appropriate conditions to obtain a target compound. The compounds are widely used in the preparation of pharmaceuticals, dyes, pesticides and other organic compounds.
Method:
The method of preparing R-N-Boc-3-amino -4-methyl valerate hydrochloride usually involves the following steps:
1. Reaction of 3-amino-4-methylpentanoic acid with the R-enantiomer of tert-butyryl chloride (tert-butyryl chloride) yields tert-butyl R-N-Boc-3-amino-4-methylpentanoate.
2. The product is reacted with hydrochloric acid to obtain R-N-Boc-3-amino-4-methylvalerate hydrochloride.
Safety Information:
R-N-Boc-3-amino -4-methyl valerate hydrochloride is less toxic and corrosive under normal operating conditions. However, as an organic compound, appropriate laboratory safety measures should be taken, including wearing appropriate protective gloves and eye protection to avoid skin contact and inhalation. If necessary, it should be operated in a well-ventilated environment and stored in a sealed container, away from fire and oxidizing agents. When handling this compound, it is recommended to refer to the relevant safety Data Sheet (MSDS) for more detailed information.
Last Update：2024-04-09 20:45:29
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CAS: 183990-64-9
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