| Identification | More | [Name]
N-Boc-L-tert-Leucine | [CAS]
62965-35-9 | [Synonyms]
BOC-ALPHA-BUTYLGLYCINE
BOC-ALPHA-T-BUTYLGLYCINE
BOC-ALPHA-T-BUTYLGLYCINE-OH
BOC-ALPHA-T-BUTYL-GLY-OH
BOC-L-ALPHA-T-BUTYLGLYCINE
BOC-L-T-BUTYLGLYCINE
BOC-L-TERT-LEUCINE
BOC-L-TLE-OH
BOC-TBU-GLYCINE
BOC-TBU-GLY-OH
BOC-TLE
BOC-TLE-OH
N-ALPHA-T-BOC-L-ALPHA-T-BUTYL-GLYCINE
N-ALPHA-T-BOC-L-T-LEUCINE
N-ALPHA-T-BUTOXYCARBONYL-L-ALPHA-T-BUTYL-GLYCINE
N-ALPHA-T-BUTOXYCARBONYL-L-T-BUTYLGLYCINE
N-ALPHA-T-BUTOXYCARBONYL-L-T-LEUCINE
N-ALPHA-T-BUTOXYCARBONYL-(S)-2-AMINO-3,3-DIMETHYL-BUTYRIC ACID
N-ALPHA-T-BUTYLOXYCARBONYL-L-T-LEUCINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-TERT-BUTYLGLYCINE | [EINECS(EC#)]
613-118-8 | [Molecular Formula]
C11H21NO4 | [MDL Number]
MFCD00065574 | [Molecular Weight]
231.29 | [MOL File]
62965-35-9.mol |
| Chemical Properties | Back Directory | [Appearance]
White crystalline powder | [Melting point ]
118-121 °C
| [alpha ]
-4.2 º (c=1% in glacial acetic acid) | [storage temp. ]
Store at RT. | [solubility ]
DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | [form ]
Crystalline Powder | [color ]
White to slightly yellow | [optical activity]
[α]20/D 4.2±0.5°, c = 1% in glacial acetic acid | [BRN ]
1962763 | [InChI]
InChI=1/C11H21NO4/c1-10(2,3)7(8(13)14)12-9(15)16-11(4,5)6/h7H,1-6H3,(H,12,15)(H,13,14)/t7-/s3 | [InChIKey]
LRFZIPCTFBPFLX-SSDOTTSWSA-N | [SMILES]
[C@@H](C(=O)O)(C(C)(C)C)NC(=O)OC(C)(C)C |&1:0,r| | [CAS DataBase Reference]
62965-35-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29241990 |
| Hazard Information | Back Directory | [Description]
N-Boc-L-tert-Leucine is a white to slightly yellow crystalline powder. The carboxyl group in its structure can be condensed with alcohol compounds under the catalysis of acid or base to obtain the corresponding ester derivatives. This substance can be used for the synthesis of amino acid drugs due to the various chemical transformation properties of its amine and carboxyl groups. The Boc protective group is able to protect the amino group of the amino acid from non-specific reactions with other reactants. This compound is a derivative of L-tert-Leucine, which is a non-polar amino acid. Its tert-butyl group exhibits significant hydrophobicity and steric hindrance, enabling effective control of molecular conformation in chemical reactions, leading to the formation of chiral compounds. As a crucial chiral intermediate, L-tert-leucine is widely employed in the synthesis of anti-cancer, anti-viral, and biological inhibitors. Additionally, L-tert-leucine serves as an essential additive in the food and cosmetic industry.
| [Chemical Properties]
White crystalline powder | [Uses]
Atazanavir Related Compound A |
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