(S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID
boc-3-cyclohexyl-L-alanine hydrate
CAS: 37736-82-6
Molecular Formula: C14H25NO4
(S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID - Names and Identifiers
| Name | boc-3-cyclohexyl-L-alanine hydrate |
| Synonyms | BOC-CHA-OH Boc-Cha-OH BOC-L-CHA-OH Boc-Cha-OH hydrate BOC-L-CYCLOHEXYLALANINE BOC-Beta-cyclohexyl-Ala-OH BOC-BETA-CYCLOHEXYL-ALA-OH BOC-3-CYCLOHEXYL-L-ALANINE Boc-(S)-3-Cyclohexylalanine BOC-BETA-CYCLOHEXYL-ALANINE Boc-.beta.-cyclohexyl-Ala-OH BOC-BETA-CYCLOHEXYL-L-ALANINE N-T-boc-B-cyclohexyl-L-alanine boc-3-cyclohexyl-L-alanine hydrate N-(tert-butoxycarbonyl)-3-cyclohexyl-L-alanine N-α-tert-Butoxycarbonyl-3-cyclohexyl-L-alanine (S)-2-Tert-Butoxycarbonylamino-3-Cyclohexylpropionic Acid? (S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID |
| CAS | 37736-82-6 |
| EINECS | 1308068-626-2 |
| InChI | InChI=1/C14H25NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h10-11H,4-9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m0/s1 |
| InChIKey | MSZQAQJBXGTSHP-NSHDSACASA-N |
(S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID - Physico-chemical Properties
| Molecular Formula | C14H25NO4 |
| Molar Mass | 271.35 |
| Density | 1.083±0.06 g/cm3(Predicted) |
| Boling Point | 420.4±28.0 °C(Predicted) |
| Flash Point | 208.07°C |
| Vapor Presure | 0mmHg at 25°C |
| BRN | 3060603 |
| pKa | 4.02±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.484 |
(S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29242990 |
| Hazard Class | IRRITANT |
(S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID - Introduction
boc-3-cyclohexyl-L-alanine hydrate(boc-3-cyclohexyl-L-alanine hydrate) is an organic compound with the following properties:
1. Appearance: White crystalline solid.
2. Molecular formula: C15H28N2O4 · HCl · H2O.
3. Molecular weight: 360.86g/mol.
4. melting point: 98-100 ℃ (decomposition).
5. Solubility: Soluble in water, slightly soluble in chloroform, almost insoluble in alcohol and ether.
The main uses of boc-3-cyclohexyl-L-alanine hydrate are as follows:
1. Chemical intermediates: can be used as an important intermediate in organic synthesis, used in the synthesis of a variety of drugs and bioactive molecules.
2. protein synthesis: as a protective group used in protein synthesis and modification.
preparation method, boc-3-cyclohexyl-L-alanine hydrate can be obtained through the following steps:
1. First, cyclohexanecarboxylic acid and N,N-dimethylethylenediamine are reacted in an appropriate solvent to produce cycloethylalanine.
2. Then, cycloethylalanine is reacted with butyric anhydride acid (BOC-ANHYDRIDE) under basic conditions to produce butoxycarbonyl-cycloethyl-alanine.
3. Finally, the butoxycarbonyl-cycloethyl-alanine is reacted with hydrochloric acid and water to produce a boc-3-cyclohexyl-L-alanine hydrate.
In terms of safety information, the specific safety information of the boc-3-cyclohexyl-L-alanine hydrate can be obtained by consulting the safety data sheet (SDS) of the compound. During use, care should be taken to prevent contact with skin, eyes and inhalation, and avoid swallowing. Wear appropriate personal protective equipment such as lab gloves, goggles and protective clothing when used.
1. Appearance: White crystalline solid.
2. Molecular formula: C15H28N2O4 · HCl · H2O.
3. Molecular weight: 360.86g/mol.
4. melting point: 98-100 ℃ (decomposition).
5. Solubility: Soluble in water, slightly soluble in chloroform, almost insoluble in alcohol and ether.
The main uses of boc-3-cyclohexyl-L-alanine hydrate are as follows:
1. Chemical intermediates: can be used as an important intermediate in organic synthesis, used in the synthesis of a variety of drugs and bioactive molecules.
2. protein synthesis: as a protective group used in protein synthesis and modification.
preparation method, boc-3-cyclohexyl-L-alanine hydrate can be obtained through the following steps:
1. First, cyclohexanecarboxylic acid and N,N-dimethylethylenediamine are reacted in an appropriate solvent to produce cycloethylalanine.
2. Then, cycloethylalanine is reacted with butyric anhydride acid (BOC-ANHYDRIDE) under basic conditions to produce butoxycarbonyl-cycloethyl-alanine.
3. Finally, the butoxycarbonyl-cycloethyl-alanine is reacted with hydrochloric acid and water to produce a boc-3-cyclohexyl-L-alanine hydrate.
In terms of safety information, the specific safety information of the boc-3-cyclohexyl-L-alanine hydrate can be obtained by consulting the safety data sheet (SDS) of the compound. During use, care should be taken to prevent contact with skin, eyes and inhalation, and avoid swallowing. Wear appropriate personal protective equipment such as lab gloves, goggles and protective clothing when used.
Last Update：2024-04-09 21:50:46
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