Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Isoleucine derivatives >  GAMMA-METHYL-L-LEUCINE

GAMMA-METHYL-L-LEUCINE

Basic information Safety Supplier Related

GAMMA-METHYL-L-LEUCINE Basic information

Product Name:
GAMMA-METHYL-L-LEUCINE
Synonyms:
  • H-L-tBuAla-OH
  • H-L-NptGly-OH=4-Methyl-L-leucine
  • L-Nepentylglycine
  • γ-methyl-l-leucine
  • gamma-methylleucine
  • L-Neopentylglycine, 4-Methyl-L-leucine, ss-t-Butyl-L-alanine, (S)-2-Amino-4,4-dimethyl-pentanoic acid
  • H-b-tBu-Ala-OH
  • γ-Methyl-L-leucine, (S)-2-Amino-4,4-dimethylpentanoic acid, L-γ-Methylleucine
CAS:
57224-50-7
MF:
C7H15NO2
MW:
145.2
Mol File:
57224-50-7.mol
More
Less

GAMMA-METHYL-L-LEUCINE Chemical Properties

Melting point:
250 - 252°C
Boiling point:
236.0±23.0℃ (760 Torr)
Density 
1.016±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
96.5±22.6℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Methanol (Slightly), Water (Sparingly)
form 
Solid
pka
2.56±0.23(Predicted)
color 
White to Off-White
optical activity
Consistent with structure
InChI
InChI=1S/C7H15NO2/c1-7(2,3)4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1
InChIKey
LPBSHGLDBQBSPI-YFKPBYRVSA-N
SMILES
C(O)(=O)[C@@H](N)CC(C)(C)C
More
Less

Safety Information

WGK Germany 
3
10

MSDS

More
Less

GAMMA-METHYL-L-LEUCINE Usage And Synthesis

Chemical Properties

White to off-white powder

Uses

Gamma-methyl-L-leucine

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

34906-87-1

3060-50-2

119-61-9

57224-50-7

88319-43-1

GENERAL STEPS: To a 5 mL reaction vial equipped with a magnetic stirrer was added 3-cyclohexyl-2-oxopropanoic acid (1j) (0.0510 g, 0.30 mmol), 2,2-diphenylglycine (2) (0.0681 g, 0.30 mmol), chiral pyridoxamine 6 g (0.0195 g, 0.030 mmol) and MeOH-H2O (8:2) , v/v) (3.0 mL). The reaction mixture was stirred at 20 °C for 3 days. Upon completion of the reaction, the mixture was transferred to a 25 mL round-bottom flask and methanol was added until all solids were completely dissolved. Silica gel (0.50 g) was then added. The solvent was removed by reduced pressure distillation at 20 °C and the resulting residue was purified by silica gel column chromatography (eluent ratio EtOH/ethyl acetate/25-28% ammonia solution = 100:58:16) to afford compound 3j (0.0401 g, 78% yield, 52% ee) as a white solid. To determine the enantiomeric excess of 3b-k, compound 3j was first treated with thionyl chloride in methanol and subsequently converted to N-benzoylmethyl ester by reaction with benzoyl chloride and finally analyzed by HPLC. For the determination of enantiomeric excess of compound 3a, it was converted to methyl ester by treatment with CH2N2 in methanol followed by HPLC analysis.

References

[1] Tetrahedron Letters, 2016, vol. 57, # 41, p. 4612 - 4615

GAMMA-METHYL-L-LEUCINESupplier

Suzhou haiyu Biochem Industrial Co., LTD Gold
Tel
512-68097639 18013585858
Email
744942877@qq.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com