| Identification | Back Directory | [Name]
BOC-ALLO-ILE-OH | [CAS]
35264-07-4 | [Synonyms]
BOC-ALLO-ILE-OH
Boc-allo-lle-OH
Boc-L-Allo-Ile-OH
Boc-allo-L-Ile-OH
BOC-ALLO-ISOLEUCINE
BOC-L-ALLOISOLEUCINE
BOC-ALLO-ILE-OH HYDRATE
Boc-L-allo-isoleucine99%
BOC-ALLO-ILE-OH USP/EP/BP
Boc-allo-Ile-OH >=99.0% (TLC)
Boc-(2S,3R)-2-amino-3-methylpentanoic acid
L-Alloisoleucine, N-[(1,1-dimethylethoxy)carbonyl]-
N-ALPHA-T-BUTOXYCARBONYL-L-ALLO-ISOLEUCINE HEMIHYDRATE
(2S,3R)-2-(tert-butoxycarbonylamino)-3-methylpentanoic acid
(2S,3R)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoicaci
(2S,3R)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid | [Molecular Formula]
C11H21NO4 | [MDL Number]
MFCD00151905 | [MOL File]
35264-07-4.mol | [Molecular Weight]
231.29 |
| Chemical Properties | Back Directory | [Melting point ]
60-64 °C | [Boiling point ]
356.0±25.0 °C(Predicted) | [density ]
1.061±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
4.03±0.22(Predicted) | [Appearance]
White to off-white Solid | [Optical Rotation]
12.1° (C=0.01 g/ml, CHCL3) | [BRN ]
2212874 | [Major Application]
peptide synthesis | [InChI]
1S/C11H21NO4/c1-6-7(2)8(9(13)14)12-10(15)16-11(3,4)5/h7-8H,6H2,1-5H3,(H,12,15)(H,13,14)/t7-,8+/m1/s1 | [InChIKey]
QJCNLJWUIOIMMF-SFYZADRCSA-N | [SMILES]
CC[C@@H](C)[C@H](NC(=O)OC(C)(C)C)C(O)=O |
| Hazard Information | Back Directory | [Uses]
Boc-allo-Ile-OH is used to prepare substituted isoindolines as inhibitors of DPP8/9. It is also used to synthesize antifungal, cyclic depsipeptide aureobasidin A. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
|
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
| Company Name: |
Shanghai GL Peptide Ltd.
|
| Telephone: |
+86-21-61263310 13764994101 |
| Website: |
www.chemicalbook.com/supplier/10480342/ |
|