Z-Ile-OH

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Names

[ CAS No. ]:
3160-59-6

[ Name ]:
Z-Ile-OH

[Synonym ]:
Z-Ile-Oh
AmbotzZAA1009
N-Cbz-L-Ile-OH
N-Carbobenzoxy-L-isoleucine
N-Cbz-isoleucine
Cbz-isoleucine
N-Carbobenzyloxy-L-isoleucine
CBZ-L-ISOLEUCINE
Z-L-Isoleucine
EINECS 221-611-0
UPCMLD00WV-81:002
MFCD00027064
N-Cbz-L-isoleucine
N-benzyloxycarbonyl-L-isoleucine
Cbz-L-isoluecine
N-Carbobenzyloxy-L-isoleucine,Z-Ile-OH
N-[(Benzyloxy)carbonyl]-L-isoleucine
Benzyloxycarbonyl-L-isoleucine

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
442.8±38.0 °C at 760 mmHg

[ Melting Point ]:
52-54 °C(lit.)

[ Molecular Formula ]:
C14H19NO4

[ Molecular Weight ]:
265.305

[ Flash Point ]:
221.6±26.8 °C

[ Exact Mass ]:
265.131409

[ PSA ]:
75.63000

[ LogP ]:
3.12

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.528

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • L-Isoleucine
  • Benzyl chloroformate
  • Z-Ile-ONP
  • Dibenzyl dicarbonate

DownStream

  • L-Isoleucine Orlistat
  • N-[(Benzyloxy)carbonyl]-N-methyl-L-isoleucine
  • Z-ILE-OSU
  • N-Methyl-L-isoleucine
  • L-Isoleucine
  • z-ile-ala-oh
  • Z-Ile-Gly-OH
  • L-Z-Isoleucinamide
  • (3R,4S)-4-methyl-3-(phenylmethoxycarbonylamino)hexanoic acid
  • H-Ile-Ile-OH

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . 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...


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Related Compounds

  • N-(4-ethoxyphenyl)-2-[7-oxo-2-(piperidin-1-yl)[1,3]thiazolo[4,5-d]pyrimidin-6(7H)-yl]acetamide
  • 2-[7-oxo-2-(piperidin-1-yl)[1,3]thiazolo[4,5-d]pyrimidin-6(7H)-yl]-N-(2,4,6-trimethylphenyl)acetamide
  • N-(4-bromo-3-methylphenyl)-2-[7-oxo-2-(piperidin-1-yl)[1,3]thiazolo[4,5-d]pyrimidin-6(7H)-yl]acetamide
  • N-(3-chloro-4-methoxyphenyl)-2-(7-oxo-2-(pyrrolidin-1-yl)thiazolo[4,5-d]pyrimidin-6(7H)-yl)acetamide
  • N-(3-chlorophenyl)-2-(7-oxo-2-(pyrrolidin-1-yl)thiazolo[4,5-d]pyrimidin-6(7H)-yl)acetamide
  • 2-(7-oxo-2-(pyrrolidin-1-yl)thiazolo[4,5-d]pyrimidin-6(7H)-yl)-N-(p-tolyl)acetamide
  • N-(4-chloro-2-(trifluoromethyl)phenyl)-2-(7-oxo-2-(pyrrolidin-1-yl)thiazolo[4,5-d]pyrimidin-6(7H)-yl)acetamide
  • N-(3-chloro-4-methoxyphenyl)-2-(7-oxo-2-thiomorpholinothiazolo[4,5-d]pyrimidin-6(7H)-yl)acetamide
  • N-(3-chlorophenyl)-2-(7-oxo-2-thiomorpholinothiazolo[4,5-d]pyrimidin-6(7H)-yl)acetamide
  • N-(3-fluoro-4-methylphenyl)-2-((5-oxo-4-(thiophen-2-ylmethyl)-4,5-dihydrothieno[2,3-e][1,2,4]triazolo[4,3-a]pyrimidin-1-yl)thio)acetamide
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