Fmoc-Ida-OH

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Names

[ CAS No. ]:
112918-82-8

[ Name ]:
Fmoc-Ida-OH

[Synonym ]:
Glycine,N-(carboxymethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]
N-(9-fluorenylmethoxycarbonyl)-iminodiacetic acid
N-Fmoc-iminodiacetic acid
I04-3777
Fmoc-iminodiacetic acid

Chemical & Physical Properties

[ Density]:
1.41g/cm3

[ Boiling Point ]:
618.4ºC at 760 mmHg

[ Melting Point ]:
213-217ºC

[ Molecular Formula ]:
C19H17NO6

[ Molecular Weight ]:
355.34100

[ Flash Point ]:
327.8ºC

[ Exact Mass ]:
355.10600

[ PSA ]:
104.14000

[ LogP ]:
2.40670

[ Vapour Pressure ]:
3.77E-16mmHg at 25°C

[ Index of Refraction ]:
1.635

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2922509090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 9-Fluorenylmethyl chloroformate
  • Iminodiacetic acid

DownStream

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Structure-activity relationships of 1,3-dialkylxanthine derivatives at rat A3 adenosine receptors.

J. Med. Chem. 37 , 3373, (1994)

1,3-Dialkylxanthine analogues containing carboxylic acid and other charged groups on 8-position substituents were synthesized. These derivatives were examined for affinity in radioligand binding assay...


More Articles

Related Compounds

  • Boc-Aeg(Fmoc)-OH
  • TRT-LYS(FMOC)-OH
  • TRT-DPR(FMOC)-OH
  • Alloc-Lys(Fmoc)-OH
  • Boc-Dap(Fmoc)-OH
  • ivDde-Lys(Fmoc)-OH
  • 1-methyl-N-(oxetan-3-yl)piperidine-3-carboxamide
  • 4-[3-(4,4-Difluoropiperidine-1-carbonyl)piperidin-1-yl]pyridine-2-carboxamide
  • 5-Fluoro-4-{4-[(6-methoxypyridin-3-yl)methyl]piperazin-1-yl}-6-(propan-2-yl)pyrimidine
  • 4-[4-(5-Bromopyridin-2-yl)piperazin-1-yl]-6-methyl-2-(methylsulfanyl)pyrimidine
  • 1-(1,2,3,4-tetrahydroquinolin-1-yl)-2-[3-(trifluoromethyl)-5H,6H,7H,8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl]ethan-1-one
  • N-{1-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]piperidin-4-yl}cyclobutanecarboxamide
  • 2-[4-(2,3-Dimethylphenyl)piperazin-1-yl]pyrimidine-4-carbonitrile
  • 5-Chloro-6-{4-[2,4-dioxo-3-(2,2,2-trifluoroethyl)imidazolidin-1-yl]piperidin-1-yl}pyridine-3-carbonitrile
  • 2-[4-(2,5-Dimethylphenyl)piperazin-1-yl]pyrimidine-4-carbonitrile
  • 2-[4-(2,5-Dimethylphenyl)piperazin-1-yl]-1-(piperidin-1-yl)ethan-1-one
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