H-Leu-OMe.HCl

Suppliers

Names

[ CAS No. ]:
7517-19-3

[ Name ]:
H-Leu-OMe.HCl

[Synonym ]:
Methyl L-leucinate hydrochloride (1:1)
L-Leucine, methyl ester, hydrochloride (1:1)
EINECS 231-375-0
L-Leucine, methyl ester, hydrochloride
MFCD00012494
methyl (2S)-2-amino-4-methylpentanoate,hydrochloride
H-Leu-OMe·HCl
H-Leu-OMe.HCl

Chemical & Physical Properties

[ Density]:
0.955 g/cm3

[ Boiling Point ]:
169.2ºC at 760 mmHg

[ Melting Point ]:
151-153 °C(lit.)

[ Molecular Formula ]:
C7H16ClNO2

[ Molecular Weight ]:
181.660

[ Exact Mass ]:
181.086960

[ PSA ]:
52.32000

[ LogP ]:
2.03510

[ Index of Refraction ]:
13 ° (C=2, H2O)

[ Storage condition ]:
0-6°C

[ Water Solubility ]:
soluble

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29224995

Synthetic Route

Precursor & DownStream

Precursor

  • Methanol
  • L-leucine
  • (2S)-methyl 2-(2-azabicyclo[2.2.1]hept-5-en-2-yl)-4-methylpentanoate
  • methyl (S)-2-methoxycarbonylamino-4-methyl-valerate
  • methyl L-leucinate
  • Z-Leu-Ome
  • 2,2-Dimethoxypropane
  • L-leucyl chloride

DownStream

  • (4R)-1-(tert-Butoxycarbonyl)-4-methyl-L-proline
  • Boc-Phe-Leu-OH
  • L-Leucine,N2-[(phenylmethoxy)carbonyl]-L-asparaginyl-, methyl ester
  • METHYL 4-METHYL-2-([(4-METHYLPHENYL)SULFONYL]AMINO)PENTANOATE
  • N-(2-Carboxy-3-phenylpropanoyl)-L-leucine
  • 2H-Pyrrol-2-one,3-acetyl-1,5-dihydro-4-hydroxy-5-(2-methylpropyl)-
  • L-leucine
  • Cbz-pro-Leu-Ome
  • Cyclo(-leu-pro)
  • Bestatin hydrochloride

Customs

[ HS Code ]: 2922499990

[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

Articles

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Targeting Btk/Etk of prostate cancer cells by a novel dual inhibitor.

Cell Death Dis. 5 , e1409, (2014)

Btk and Etk/BMX are Tec-family non-receptor tyrosine kinases. Btk has previously been reported to be expressed primarily in B cells and has an important role in immune responses and B-cell malignancie...

Primary in vitro immunization with multimeric synthetic peptides of HIV-1 envelope glycoproteins: generation of neutralizing human monoclonal antibodies.

J. Immunol. Methods 176(1) , 9-22, (1994)

Peripheral blood lymphocytes from healthy HIV-1 seronegative donors were immunized in vitro with the following synthetic peptides: (i) an octameric poly-L-lysine conjugated peptide of the HIV-1MN V3 l...


More Articles


Related Compounds

  • H-DL-Leu-Ome.HCl
  • H-D-Leu-OMe.HCl
  • H-Leu-Met-OCH3
  • H-Leu-Met-Ala-Phe-Ile-Gly-OH*HCl
  • H-Leu-Arg-Arg-Ile-N2H2Ph
  • H-Leu-Gly-OBzl*HCl
  • 1-cyclopropyl-3-((1-methyl-1H-imidazol-2-yl)thio)pyrazin-2(1H)-one
  • 1-methyl-4-(((1-methyl-1H-imidazol-2-yl)thio)methyl)pyrrolidin-2-one
  • 2,4-Dimethyl-6-(pyridin-2-ylthio)pyrimidine
  • 5-methyl-N-(oxan-4-yl)pyrazolo[1,5-a]pyrimidin-7-amine
  • 2-((pyridin-3-ylmethyl)amino)-4H-pyrido[1,2-a]pyrimidin-4-one
  • 4-{[(1R,2R)-2-hydroxycyclopentyl]oxy}phenol
  • 3,4-dimethoxy-N-methyl-N-(1-{[1,2,4]triazolo[4,3-b]pyridazin-6-yl}azetidin-3-yl)benzamide
  • N-(1-([1,2,4]triazolo[4,3-b]pyridazin-6-yl)azetidin-3-yl)-N-methylpicolinamide
  • 2-(2-methoxyphenyl)-N-methyl-N-(1-{[1,2,4]triazolo[4,3-b]pyridazin-6-yl}azetidin-3-yl)acetamide
  • N-(1-([1,2,4]triazolo[4,3-b]pyridazin-6-yl)azetidin-3-yl)-N,5-dimethyl-1-phenyl-1H-pyrazole-4-carboxamide
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.