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ChemicalBook--->CAS DataBase List--->84000-07-7

84000-07-7

84000-07-7 Structure

84000-07-7 Structure
IdentificationMore
[Name]

FMOC-N-Methyl-L-alanine
[CAS]

84000-07-7
[Synonyms]

FMOC-L-MEALA-OH
FMOC-MEALA-OH
FMOC-N-ALPHA-METHYL-L-ALANINE
FMOC-N-ME-ALA-OH
FMOC-N-ME-L-ALA-OH
FMOC-N-METHYL-L-ALANINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-ALPHA-METHYL-L-ALANINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-L-ALANINE
N-ALPHA-FMOC-N-ALPHA-METHYL-L-ALANINE
FMOC-N-ME-ALA 98.5+%
Fmoc-N-Me-Ala-OH Fmoc-N-methyl-L-Alanine
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C19H19NO4
[MDL Number]

MFCD00153384
[Molecular Weight]

325.36
[MOL File]

84000-07-7.mol
Chemical PropertiesBack Directory
[Melting point ]

~150 °C
[alpha ]

-18.5 º (c=1,DMF)
[Boiling point ]

514.9±29.0 °C(Predicted)
[density ]

1.262±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Soluble in water or 1% acetic acid
[form ]

Solid
[pka]

3.92±0.10(Predicted)
[color ]

White to Almost white
[Optical Rotation]

[α]20/D 18.5±1°, c = 1% in DMF
[Water Solubility ]

Slightly soluble in water.
[BRN ]

4329998
[Sequence]

Fmoc-N-Me-Ala-OH
[InChIKey]

JOFHWKQIQLPZTC-LBPRGKRZSA-N
[CAS DataBase Reference]

84000-07-7(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[HS Code ]

2924 29 70
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Chemical Properties]

White to off white powder
[Uses]

It is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field. Also used in N-methyl amino acids for peptide synthesis.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
[Synthesis]

3-Oxazolidinecarboxylic acid, 4-methyl-5-oxo-, 9H-fluoren-9-ylmethyl ester, (4S)-

83999-95-5

FMOC-N-Methyl-L-alanine

84000-07-7

The general procedure for the synthesis of Fmoc-N-methyl-L-alanine from the compound (CAS: 83999-95-5) was as follows: paraformaldehyde (4.0 g, 133 mmol) and p-toluenesulfonic acid (0.5 g, 13.3 mmol) were added to a suspension of Fmoc-L-alanine (6.2 g, 19.9 mmol) in toluene (400 mL). The mixture was refluxed for 30 min to remove azeotropic water. The solution was cooled, washed with 1 M aqueous NaHCO3 (2 x 100 mL) and dried with Na2SO4. Subsequently, the solution was concentrated in vacuum to give a white solid. The above oxazolidinone was dissolved in chloroform (75 mL) and trifluoroacetic acid (75 mL) and triethylsilane (7.2 mL, 44.8 mmol) were added. The reaction mixture was stirred at room temperature for 10 hours and then concentrated under vacuum. The resulting oily substance was dissolved in dichloromethane and the concentration was repeated three times. After standing, the oily substance crystallized. The crystals were redissolved in ether and concentrated. Finally, the collected white solid was washed with 5% ether/hexane and dried to give the product (6.1 g, 94% yield).

[References]

[1] Tetrahedron Letters, 2011, vol. 52, # 30, p. 3872 - 3875
[2] European Journal of Organic Chemistry, 2013, # 21, p. 4509 - 4513
[3] Journal of Organic Chemistry, 2005, vol. 70, # 17, p. 6918 - 6920
[4] Tetrahedron Letters, 2006, vol. 47, # 11, p. 1691 - 1694
[5] Tetrahedron Letters, 2014, vol. 55, # 44, p. 6109 - 6112
Spectrum DetailBack Directory
[Spectrum Detail]

FMOC-N-Methyl-L-alanine(84000-07-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

84000-07-7(sigmaaldrich)
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