| Identification | Back Directory | [Name]
BOC-L-LEUCINE N,O-DIMETHYLHYDROXAMIDE | [CAS]
87694-52-8 | [Synonyms]
BOC-VAL-NME(OME)
BOC-LEU-NME(OME)
BOC-LEU-N(OME)ME
Boc-Val-N(MMe)Me
BOC-VAL-N(OCH3)CH3
Boc-L-Val-N(OCH3)CH3
BOC-L-VALINE N,O-DIMETHYLHYDROXAMIDE
BOC-L-LEUCINE N,O-DIMETHYLHYDROXAMIDE
BOC-L-VALINE N-METHOXY-N-METHYL AMIDE
N-Boc-L-valine N'-methoxy-N'-methylamide
N-ALPHA-T-BOC-L-VALINE N-METHOXY-N-METHYL AMIDE
BOC-L-LEUCINE N,O-DIMETHYLHYDROXAMIDE USP/EP/BP
N-(tert-butoxycarbonyl)-L-valine N'-methoxy-N'-me
(S)-2-(Boc-aMino)-N-Methoxy-N,3-diMethylbutanaMide
N-(TERT-BUTOXYCARBONYL)-L-VALINE N'-METHOXY-N'-METHYLAMIDE
N-(TERT-BUTOXYCARBONYL)-L-LEUCINE N'-METHOXY-N'-METHYLAMIDE
Boc-L-valineN-methoxy-N-methyl amide≥ 98% (HPLC, Chiral purity)
tert-butyl (S)-1-(N-methoxy-N-methylcarbamoyl)-2-methylpropylcarbamate
tert-butyl N-[(2S)-1-[methoxy(methyl)amino]-3-methyl-1-oxobutan-2-yl]carbamate
N-[(1S)-1-[(Methoxymethylamino)carbonyl]-2-methylpropyl]carbamic acid tert-butyl ester
Carbamic acid,[(1S)-1-[(methoxymethylamino)carbonyl]-2-methylpropyl]-,1,1-dimethylethyl ester
Carbamic acid, N-[(1S)-1-[(methoxymethylamino)carbonyl]-2-methylpropyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C12H24N2O4 | [MDL Number]
MFCD00151875 | [MOL File]
87694-52-8.mol | [Molecular Weight]
260.33 |
| Chemical Properties | Back Directory | [Boiling point ]
235 °C(lit.)
| [density ]
1.46 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.454(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Sealed in dry,2-8°C | [form ]
Low Melting Solid or Liquid | [pka]
11.11±0.46(Predicted) | [color ]
White to pale yellow | [Optical Rotation]
[α]23/D 18.5°, c = 1 in methanol | [Major Application]
peptide synthesis | [InChI]
InChI=1/C12H24N2O4/c1-8(2)9(10(15)14(6)17-7)13-11(16)18-12(3,4)5/h8-9H,1-7H3,(H,13,16)/t9-/s3 | [InChIKey]
RRBFCGUIFHFYQK-DJEYLCQNNA-N | [SMILES]
C(OC(C)(C)C)(=O)N[C@H](C(N(OC)C)=O)C(C)C |&1:8,r| |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white crystalline powder | [Uses]
α-Amino Weinreb amide. | [Uses]
Reduced by LiAlH4 to give the corresponding Boc amino acid aldehyde. | [reaction suitability]
reaction type: solution phase peptide synthesis |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| 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 |
|